| 126727467 | CV1003111 | single nucleotide variant | NM_001318895.3(FHL2):c.689-2A>G | Primary dilated cardiomyopathy [RCV001312282] | uncertain significance | 2 | 105361436 | 105361436 | Human | 1 | name |
| 127281832 | CV1089480 | single nucleotide variant | NM_001318895.3(FHL2):c.156+8C>T | Primary dilated cardiomyopathy [RCV001447406] | likely benign | 2 | 105386353 | 105386353 | Human | 1 | name |
| 127304467 | CV1131878 | single nucleotide variant | NM_001318895.3(FHL2):c.688+7G>A | Primary dilated cardiomyopathy [RCV001479506] | likely benign | 2 | 105363278 | 105363278 | Human | 1 | name |
| 127304810 | CV1153773 | single nucleotide variant | NM_001318895.3(FHL2):c.332-7A>G | Primary dilated cardiomyopathy [RCV001516051] | benign | 2 | 105367746 | 105367746 | Human | 1 | name |
| 151875303 | CV1376075 | single nucleotide variant | NM_001318895.3(FHL2):c.157-3C>T | Primary dilated cardiomyopathy [RCV002019464] | uncertain significance | 2 | 105373736 | 105373736 | Human | 1 | name |
| 151872339 | CV1470748 | single nucleotide variant | NM_001318895.3(FHL2):c.502-1G>C | Primary dilated cardiomyopathy [RCV001925384] | uncertain significance | 2 | 105363472 | 105363472 | Human | 1 | name |
| 152064509 | CV1535814 | single nucleotide variant | NM_001318895.3(FHL2):c.502-5T>C | Primary dilated cardiomyopathy [RCV002168447] | likely benign | 2 | 105363476 | 105363476 | Human | 1 | name |
| 9691656 | CV172794 | single nucleotide variant | NM_001318895.3(FHL2):c.156+2T>C | not specified [RCV000150709] | uncertain significance | 2 | 105386359 | 105386359 | Human | | name |
| 155911355 | CV2029276 | single nucleotide variant | NM_001318895.3(FHL2):c.501+8A>T | Primary dilated cardiomyopathy [RCV002750163] | likely benign | 2 | 105367562 | 105367562 | Human | 1 | name |
| 402523942 | CV2887520 | single nucleotide variant | NM_001318895.3(FHL2):c.501+5C>G | Primary dilated cardiomyopathy [RCV003511061] | uncertain significance | 2 | 105367565 | 105367565 | Human | 1 | name |
| 405159353 | CV3001460 | single nucleotide variant | NM_001318895.3(FHL2):c.501+6T>C | Primary dilated cardiomyopathy [RCV003621032] | uncertain significance | 2 | 105367564 | 105367564 | Human | 1 | name |
| 405141420 | CV3035201 | single nucleotide variant | NM_001318895.3(FHL2):c.157-9G>A | Primary dilated cardiomyopathy [RCV003619335] | likely benign | 2 | 105373742 | 105373742 | Human | 1 | name |
| 404982589 | CV3184220 | single nucleotide variant | NM_001318895.3(FHL2):c.331+6G>A | Primary dilated cardiomyopathy [RCV003880712] | uncertain significance | 2 | 105373553 | 105373553 | Human | 1 | name |
| 597935994 | CV3759507 | single nucleotide variant | NM_001318895.3(FHL2):c.157-8C>T | Primary dilated cardiomyopathy [RCV005076627] | likely benign | 2 | 105373741 | 105373741 | Human | 1 | name |
| 597869376 | CV3798550 | single nucleotide variant | NM_001318895.3(FHL2):c.332-6T>C | Primary dilated cardiomyopathy [RCV005144138] | likely benign | 2 | 105367745 | 105367745 | Human | 1 | name |
| 15195893 | CV759100 | single nucleotide variant | NM_001318895.3(FHL2):c.156+9T>C | Primary dilated cardiomyopathy [RCV000911544] | likely benign | 2 | 105386352 | 105386352 | Human | 1 | name |
| 28897722 | CV904034 | single nucleotide variant | NM_001318895.3(FHL2):c.332-6T>A | Cardiomyopathy [RCV001171210]|Primary dilated cardiomyopathy [RCV001859104] | uncertain significance | 2 | 105367745 | 105367745 | Human | 3 | name |
| 152081037 | CV1546660 | single nucleotide variant | NM_001318895.3(FHL2):c.156+11C>T | Primary dilated cardiomyopathy [RCV002130817] | likely benign | 2 | 105386350 | 105386350 | Human | 1 | name |
| 152161558 | CV1555440 | single nucleotide variant | NM_001318895.3(FHL2):c.688+11C>T | Primary dilated cardiomyopathy [RCV002103895] | likely benign | 2 | 105363274 | 105363274 | Human | 1 | name |
| 152069303 | CV1569912 | single nucleotide variant | NM_001318895.3(FHL2):c.157-14G>A | Primary dilated cardiomyopathy [RCV002191564] | likely benign | 2 | 105373747 | 105373747 | Human | 1 | name |
| 152095411 | CV1575215 | single nucleotide variant | NM_001318895.3(FHL2):c.502-11C>T | Primary dilated cardiomyopathy [RCV002132559] | likely benign | 2 | 105363482 | 105363482 | Human | 1 | name |
| 152049732 | CV1618595 | single nucleotide variant | NM_001318895.3(FHL2):c.501+17C>T | Primary dilated cardiomyopathy [RCV002166717] | likely benign | 2 | 105367553 | 105367553 | Human | 1 | name |
| 152158155 | CV1630700 | single nucleotide variant | NM_001318895.3(FHL2):c.331+16T>C | Primary dilated cardiomyopathy [RCV002122727]|not provided [RCV004710408] | benign | 2 | 105373543 | 105373543 | Human | 1 | name |
| 152044477 | CV1637850 | single nucleotide variant | NM_001318895.3(FHL2):c.502-16C>T | Primary dilated cardiomyopathy [RCV002144923] | likely benign | 2 | 105363487 | 105363487 | Human | 1 | name |
| 156130010 | CV1889362 | single nucleotide variant | NM_001318895.3(FHL2):c.502-10G>A | Primary dilated cardiomyopathy [RCV003081798] | likely benign | 2 | 105363481 | 105363481 | Human | 1 | name |
| 156051251 | CV1923918 | single nucleotide variant | NM_001318895.3(FHL2):c.501+16C>T | Primary dilated cardiomyopathy [RCV002637944] | likely benign | 2 | 105367554 | 105367554 | Human | 1 | name |
| 155996312 | CV2122600 | single nucleotide variant | NM_001318895.3(FHL2):c.502-13C>G | Primary dilated cardiomyopathy [RCV002974969] | likely benign | 2 | 105363484 | 105363484 | Human | 1 | name |
| 402513599 | CV2925404 | single nucleotide variant | NM_001318895.3(FHL2):c.502-12T>C | Primary dilated cardiomyopathy [RCV003510200] | likely benign | 2 | 105363483 | 105363483 | Human | 1 | name |
| 405157235 | CV2978383 | single nucleotide variant | NM_001318895.3(FHL2):c.331+10C>A | Primary dilated cardiomyopathy [RCV003620861] | likely benign | 2 | 105373549 | 105373549 | Human | 1 | name |
| 405185597 | CV3160153 | single nucleotide variant | NM_001318895.3(FHL2):c.332-14G>T | Primary dilated cardiomyopathy [RCV003859208] | likely benign | 2 | 105367753 | 105367753 | Human | 1 | name |
| 597962096 | CV3753599 | single nucleotide variant | NM_001318895.3(FHL2):c.502-13C>T | Primary dilated cardiomyopathy [RCV005081903] | likely benign | 2 | 105363484 | 105363484 | Human | 1 | name |
| 597851193 | CV3781879 | single nucleotide variant | NM_001318895.3(FHL2):c.501+20G>C | Primary dilated cardiomyopathy [RCV005126307] | likely benign | 2 | 105367550 | 105367550 | Human | 1 | name |
| 597865132 | CV3791996 | single nucleotide variant | NM_001318895.3(FHL2):c.332-11C>T | Primary dilated cardiomyopathy [RCV005139552] | likely benign | 2 | 105367750 | 105367750 | Human | 1 | name |
| 598201980 | CV3891266 | single nucleotide variant | NM_001318895.3(FHL2):c.157-12C>G | not provided [RCV005255083] | uncertain significance | 2 | 105373745 | 105373745 | Human | | name |
| 8611188 | CV57489 | single nucleotide variant | NM_001318895.3(FHL2):c.688+12G>T | Primary dilated cardiomyopathy [RCV002054834]|not provided [RCV001668173]|not specified [RCV000041648] | benign | 2 | 105363273 | 105363273 | Human | 1 | name |
| 8611189 | CV57490 | single nucleotide variant | NM_001318895.3(FHL2):c.689-10C>G | Cardiomyopathy [RCV000768813]|Primary dilated cardiomyopathy [RCV000458869]|not specified [RCV000041649] | benign | 2 | 105361444 | 105361444 | Human | 3 | name |
| 8611190 | CV57491 | single nucleotide variant | NM_001318895.3(FHL2):c.689-12C>G | Primary dilated cardiomyopathy [RCV002054835]|not provided [RCV000834018]|not specified [RCV000041650] | benign | 2 | 105361446 | 105361446 | Human | 1 | name |
| 150448072 | CV1261915 | single nucleotide variant | NM_001318895.3(FHL2):c.688+236A>G | not provided [RCV001680300] | benign | 2 | 105363049 | 105363049 | Human | | name |
| 150446935 | CV1271944 | single nucleotide variant | NM_001318895.3(FHL2):c.331+300C>T | not provided [RCV001691358] | benign | 2 | 105373259 | 105373259 | Human | | name |
| 150444090 | CV1277945 | single nucleotide variant | NM_001318895.3(FHL2):c.502-240G>A | not provided [RCV001707088] | benign | 2 | 105363711 | 105363711 | Human | | name |
| 155267529 | CV1704971 | single nucleotide variant | NM_001318895.3(FHL2):c.689-225G>A | not provided [RCV002285576] | likely benign | 2 | 105361659 | 105361659 | Human | | name |
| 402504301 | CV2899236 | deletion | NM_001318895.3(FHL2):c.332-11_332-3del | Primary dilated cardiomyopathy [RCV003509101] | likely benign | 2 | 105367742 | 105367750 | Human | 1 | name |
| 156158832 | CV2095048 | single nucleotide variant | NM_001318895.3(FHL2):c.4A>G (p.Thr2Ala) | FHL2-related disorder [RCV003427513]|Primary dilated cardiomyopathy [RCV002890910] | uncertain significance | 2 | 105386513 | 105386513 | Human | 1 | name , trait , alternate_id |
| 402507025 | CV2918584 | single nucleotide variant | NM_001318895.3(FHL2):c.72G>A (p.Glu24=) | Primary dilated cardiomyopathy [RCV003509384] | likely benign | 2 | 105386445 | 105386445 | Human | 1 | name |
| 405147190 | CV2946028 | single nucleotide variant | NM_001318895.3(FHL2):c.2T>C (p.Met1Thr) | Primary dilated cardiomyopathy [RCV003620007] | uncertain significance | 2 | 105386515 | 105386515 | Human | 1 | name |
| 408384812 | CV3503641 | single nucleotide variant | NM_001318895.3(FHL2):c.2T>A (p.Met1Lys) | FHL2-related disorder [RCV004732133] | uncertain significance | 2 | 105386515 | 105386515 | Human | | name , trait , alternate_id |
| 13493738 | CV448442 | single nucleotide variant | NM_001318895.3(FHL2):c.33C>T (p.Asn11=) | Primary dilated cardiomyopathy [RCV000558402] | likely benign | 2 | 105386484 | 105386484 | Human | 1 | name |
| 13530284 | CV496666 | single nucleotide variant | NM_001318895.3(FHL2):c.84C>T (p.Cys28=) | Cardiomyopathy [RCV001171213]|Primary dilated cardiomyopathy [RCV001402740]|not specified [RCV000600642] | benign|likely benign | 2 | 105386433 | 105386433 | Human | 3 | name |
| 126770292 | CV1003115 | single nucleotide variant | NM_001318895.3(FHL2):c.11G>C (p.Arg4Pro) | Primary dilated cardiomyopathy [RCV001322485] | uncertain significance | 2 | 105386506 | 105386506 | Human | 1 | name |
| 127281781 | CV1089479 | single nucleotide variant | NM_001318895.3(FHL2):c.285C>T (p.Asn95=) | Primary dilated cardiomyopathy [RCV001447356] | likely benign | 2 | 105373605 | 105373605 | Human | 1 | name |
| 152075855 | CV1604427 | single nucleotide variant | NM_001318895.3(FHL2):c.261G>C (p.Leu87=) | Primary dilated cardiomyopathy [RCV002092208] | likely benign | 2 | 105373629 | 105373629 | Human | 1 | name |
| 9689252 | CV172793 | single nucleotide variant | NM_001318895.3(FHL2):c.207G>A (p.Ser69=) | Cardiomyopathy [RCV001171211]|FHL2-related disorder [RCV003965150]|Primary dilated cardiomyopathy [RCV002056057]|not specified [RCV000154722] | benign|likely benign | 2 | 105373683 | 105373683 | Human | 3 | name , trait , alternate_id |
| 9687778 | CV172934 | single nucleotide variant | NM_001318895.3(FHL2):c.174C>T (p.Asp58=) | Cardiomyopathy [RCV000768818]|Primary dilated cardiomyopathy [RCV000862093]|not specified [RCV000150708] | likely benign | 2 | 105373716 | 105373716 | Human | 3 | name |
| 156228186 | CV2140791 | single nucleotide variant | NM_001318895.3(FHL2):c.243T>C (p.Ala81=) | Primary dilated cardiomyopathy [RCV003007641] | likely benign | 2 | 105373647 | 105373647 | Human | 1 | name |
| 402524323 | CV2881260 | single nucleotide variant | NM_001318895.3(FHL2):c.10C>A (p.Arg4Ser) | Primary dilated cardiomyopathy [RCV003511093] | uncertain significance | 2 | 105386507 | 105386507 | Human | 1 | name |
| 405150700 | CV3073076 | single nucleotide variant | NM_001318895.3(FHL2):c.270A>G (p.Thr90=) | Primary dilated cardiomyopathy [RCV003620338] | likely benign | 2 | 105373620 | 105373620 | Human | 1 | name |
| 597908542 | CV3845733 | single nucleotide variant | NM_001318895.3(FHL2):c.105G>A (p.Leu35=) | Primary dilated cardiomyopathy [RCV005183528] | likely benign | 2 | 105386412 | 105386412 | Human | 1 | name |
| 597917083 | CV3848974 | single nucleotide variant | NM_001318895.3(FHL2):c.252G>A (p.Glu84=) | Primary dilated cardiomyopathy [RCV005191975] | likely benign | 2 | 105373638 | 105373638 | Human | 1 | name |
| 13489652 | CV448570 | single nucleotide variant | NM_001318895.3(FHL2):c.108C>T (p.Phe36=) | Cardiomyopathy [RCV000769833]|Primary dilated cardiomyopathy [RCV000533031]|not provided [RCV004708925] | benign | 2 | 105386409 | 105386409 | Human | 3 | name |
| 8611181 | CV57482 | single nucleotide variant | NM_001318895.3(FHL2):c.120C>T (p.Cys40=) | Primary dilated cardiomyopathy [RCV000232934]|not specified [RCV000041641] | benign | 2 | 105386397 | 105386397 | Human | 1 | name |
| 8611182 | CV57483 | single nucleotide variant | NM_001318895.3(FHL2):c.192C>T (p.Ala64=) | FHL2-related disorder [RCV003915001]|Primary dilated cardiomyopathy [RCV000531538]|not provided [RCV004710470]|not specified [RCV000041642] | benign|likely benign | 2 | 105373698 | 105373698 | Human | 1 | name , trait , alternate_id |
| 14688782 | CV614742 | single nucleotide variant | NM_001318895.3(FHL2):c.141C>T (p.Ile47=) | Cardiomyopathy [RCV000769832]|Primary dilated cardiomyopathy [RCV002067212] | likely benign | 2 | 105386376 | 105386376 | Human | 3 | name |
| 15132155 | CV690687 | single nucleotide variant | NM_001318895.3(FHL2):c.186T>C (p.His62=) | Primary dilated cardiomyopathy [RCV001413477] | likely benign | 2 | 105373704 | 105373704 | Human | 1 | name |
| 15180198 | CV762134 | single nucleotide variant | NM_001318895.3(FHL2):c.291C>T (p.Tyr97=) | Primary dilated cardiomyopathy [RCV000929826] | likely benign | 2 | 105373599 | 105373599 | Human | 1 | name |
| 126725971 | CV987850 | duplication | NM_001318895.3(FHL2):c.73dup (p.Ser25fs) | Primary dilated cardiomyopathy [RCV001302746] | uncertain significance | 2 | 105386443 | 105386444 | Human | 1 | name |
| 126910188 | CV1040441 | single nucleotide variant | NM_001318895.3(FHL2):c.72G>C (p.Glu24Asp) | Primary dilated cardiomyopathy [RCV001362954] | uncertain significance | 2 | 105386445 | 105386445 | Human | 1 | name |
| 126910250 | CV1040442 | single nucleotide variant | NM_001318895.3(FHL2):c.29G>A (p.Cys10Tyr) | Primary dilated cardiomyopathy [RCV001373025] | uncertain significance | 2 | 105386488 | 105386488 | Human | 1 | name |
| 127242916 | CV1089478 | single nucleotide variant | NM_001318895.3(FHL2):c.675C>A (p.Thr225=) | Primary dilated cardiomyopathy [RCV001434734] | likely benign | 2 | 105363298 | 105363298 | Human | 1 | name |
| 127338167 | CV1131877 | single nucleotide variant | NM_001318895.3(FHL2):c.735T>C (p.His245=) | Primary dilated cardiomyopathy [RCV001493638] | likely benign | 2 | 105361388 | 105361388 | Human | 1 | name |
| 127331484 | CV1131879 | single nucleotide variant | NM_001318895.3(FHL2):c.333T>C (p.Gly111=) | Primary dilated cardiomyopathy [RCV001488827] | likely benign | 2 | 105367738 | 105367738 | Human | 1 | name |
| 150499133 | CV1235681 | duplication | NM_001318895.3(FHL2):c.688+139_688+142dup | not provided [RCV001656364] | benign | 2 | 105363142 | 105363143 | Human | | name |
| 151884560 | CV1366811 | single nucleotide variant | NM_001318895.3(FHL2):c.651T>C (p.Tyr217=) | Primary dilated cardiomyopathy [RCV001941754] | likely benign | 2 | 105363322 | 105363322 | Human | 1 | name |
| 151836541 | CV1375161 | single nucleotide variant | NM_001318895.3(FHL2):c.720G>A (p.Glu240=) | Primary dilated cardiomyopathy [RCV001921041] | likely benign|uncertain significance | 2 | 105361403 | 105361403 | Human | 1 | name |
| 152108692 | CV1530008 | single nucleotide variant | NM_001318895.3(FHL2):c.540C>T (p.Pro180=) | Primary dilated cardiomyopathy [RCV002196489] | likely benign | 2 | 105363433 | 105363433 | Human | 1 | name |
| 152151820 | CV1530587 | single nucleotide variant | NM_001318895.3(FHL2):c.816C>T (p.Cys272=) | Primary dilated cardiomyopathy [RCV002102342] | likely benign | 2 | 105361307 | 105361307 | Human | 1 | name |
| 152068601 | CV1585776 | single nucleotide variant | NM_001318895.3(FHL2):c.738C>T (p.Asn246=) | Primary dilated cardiomyopathy [RCV002147769] | likely benign | 2 | 105361385 | 105361385 | Human | 1 | name |
| 152092895 | CV1593234 | single nucleotide variant | NM_001318895.3(FHL2):c.609C>T (p.Arg203=) | Primary dilated cardiomyopathy [RCV002094434] | likely benign | 2 | 105363364 | 105363364 | Human | 1 | name |
| 152158853 | CV1595245 | single nucleotide variant | NM_001318895.3(FHL2):c.336C>T (p.Thr112=) | Primary dilated cardiomyopathy [RCV002103406] | likely benign | 2 | 105367735 | 105367735 | Human | 1 | name |
| 152129736 | CV1630828 | single nucleotide variant | NM_001318895.3(FHL2):c.759G>A (p.Lys253=) | Primary dilated cardiomyopathy [RCV002118923] | likely benign | 2 | 105361364 | 105361364 | Human | 1 | name |
| 9691657 | CV172795 | single nucleotide variant | NM_001318895.3(FHL2):c.81C>A (p.Tyr27Ter) | Primary dilated cardiomyopathy [RCV001850048]|not specified [RCV000150710] | uncertain significance | 2 | 105386436 | 105386436 | Human | 1 | name |
| 155998354 | CV1872609 | single nucleotide variant | NM_001318895.3(FHL2):c.56A>G (p.Tyr19Cys) | Primary dilated cardiomyopathy [RCV003076458]|not specified [RCV004917817] | uncertain significance | 2 | 105386461 | 105386461 | Human | 1 | name |
| 156014164 | CV1876894 | single nucleotide variant | NM_001318895.3(FHL2):c.612T>C (p.Asp204=) | Primary dilated cardiomyopathy [RCV003077264] | likely benign | 2 | 105363361 | 105363361 | Human | 1 | name |
| 156286357 | CV2001745 | single nucleotide variant | NM_001318895.3(FHL2):c.429C>T (p.Pro143=) | Primary dilated cardiomyopathy [RCV002647024] | likely benign | 2 | 105367642 | 105367642 | Human | 1 | name |
| 156156516 | CV2118203 | single nucleotide variant | NM_001318895.3(FHL2):c.86T>C (p.Val29Ala) | Primary dilated cardiomyopathy [RCV002929087]|not specified [RCV004917809] | uncertain significance | 2 | 105386431 | 105386431 | Human | 1 | name |
| 155939201 | CV2119694 | single nucleotide variant | NM_001318895.3(FHL2):c.82T>C (p.Cys28Arg) | Primary dilated cardiomyopathy [RCV002971164] | uncertain significance | 2 | 105386435 | 105386435 | Human | 1 | name |
| 156159407 | CV2138998 | single nucleotide variant | NM_001318895.3(FHL2):c.486C>T (p.Cys162=) | Primary dilated cardiomyopathy [RCV002982943] | likely benign | 2 | 105367585 | 105367585 | Human | 1 | name |
| 156350047 | CV2189534 | single nucleotide variant | NM_001318895.3(FHL2):c.56A>T (p.Tyr19Phe) | Primary dilated cardiomyopathy [RCV003048263] | uncertain significance | 2 | 105386461 | 105386461 | Human | 1 | name |
| 155966856 | CV2329849 | single nucleotide variant | NM_001318895.3(FHL2):c.64C>T (p.Arg22Trp) | Primary dilated cardiomyopathy [RCV003509772]|not specified [RCV004183309] | uncertain significance | 2 | 105386453 | 105386453 | Human | 1 | name |
| 329371251 | CV2458050 | single nucleotide variant | NM_001318895.3(FHL2):c.62T>G (p.Leu21Arg) | not specified [RCV004271883] | uncertain significance | 2 | 105386455 | 105386455 | Human | | name |
| 402522103 | CV2880075 | single nucleotide variant | NM_001318895.3(FHL2):c.336C>G (p.Thr112=) | Primary dilated cardiomyopathy [RCV003510895] | benign | 2 | 105367735 | 105367735 | Human | 1 | name |
| 402504688 | CV2902317 | single nucleotide variant | NM_001318895.3(FHL2):c.65G>A (p.Arg22Gln) | Primary dilated cardiomyopathy [RCV003509138] | uncertain significance | 2 | 105386452 | 105386452 | Human | 1 | name |
| 405160813 | CV3004214 | single nucleotide variant | NM_001318895.3(FHL2):c.414C>T (p.Thr138=) | Primary dilated cardiomyopathy [RCV003621184] | likely benign | 2 | 105367657 | 105367657 | Human | 1 | name |
| 405164331 | CV3026011 | single nucleotide variant | NM_001318895.3(FHL2):c.74G>A (p.Ser25Asn) | Primary dilated cardiomyopathy [RCV003621484] | uncertain significance | 2 | 105386443 | 105386443 | Human | 1 | name |
| 405149290 | CV3064035 | single nucleotide variant | NM_001318895.3(FHL2):c.513G>C (p.Thr171=) | Primary dilated cardiomyopathy [RCV003620181] | likely benign | 2 | 105363460 | 105363460 | Human | 1 | name |
| 405151987 | CV3076594 | single nucleotide variant | NM_001318895.3(FHL2):c.687C>T (p.Ser229=) | Primary dilated cardiomyopathy [RCV003620419] | uncertain significance | 2 | 105363286 | 105363286 | Human | 1 | name |
| 405779483 | CV3250534 | single nucleotide variant | NM_001318895.3(FHL2):c.55T>C (p.Tyr19His) | not specified [RCV004386407] | uncertain significance | 2 | 105386462 | 105386462 | Human | | name |
| 408384404 | CV3505272 | single nucleotide variant | NM_001318895.3(FHL2):c.558C>T (p.Phe186=) | FHL2-related disorder [RCV004731784]|Primary dilated cardiomyopathy [RCV005103623] | likely benign|uncertain significance | 2 | 105363415 | 105363415 | Human | 1 | name , trait , alternate_id |
| 597752974 | CV3669491 | single nucleotide variant | NM_001318895.3(FHL2):c.53A>G (p.Lys18Arg) | not specified [RCV004924034] | uncertain significance | 2 | 105386464 | 105386464 | Human | | name |
| 597881518 | CV3816012 | single nucleotide variant | NM_001318895.3(FHL2):c.594G>A (p.Gln198=) | Primary dilated cardiomyopathy [RCV005156593] | likely benign | 2 | 105363379 | 105363379 | Human | 1 | name |
| 597889368 | CV3830430 | single nucleotide variant | NM_001318895.3(FHL2):c.354G>A (p.Lys118=) | Primary dilated cardiomyopathy [RCV005164570] | likely benign | 2 | 105367717 | 105367717 | Human | 1 | name |
| 597894116 | CV3832149 | single nucleotide variant | NM_001318895.3(FHL2):c.525T>C (p.Thr175=) | Primary dilated cardiomyopathy [RCV005168885] | likely benign | 2 | 105363448 | 105363448 | Human | 1 | name |
| 597917551 | CV3843514 | single nucleotide variant | NM_001318895.3(FHL2):c.711C>A (p.Ile237=) | Primary dilated cardiomyopathy [RCV005192551] | likely benign | 2 | 105361412 | 105361412 | Human | 1 | name |
| 597919682 | CV3855600 | single nucleotide variant | NM_001318895.3(FHL2):c.567C>T (p.Thr189=) | Primary dilated cardiomyopathy [RCV005194579] | likely benign | 2 | 105363406 | 105363406 | Human | 1 | name |
| 12892595 | CV391586 | single nucleotide variant | NM_001318895.3(FHL2):c.414C>A (p.Thr138=) | Primary dilated cardiomyopathy [RCV001489585] | likely benign | 2 | 105367657 | 105367657 | Human | 1 | name |
| 12912986 | CV421265 | single nucleotide variant | NM_001318895.3(FHL2):c.513G>A (p.Thr171=) | Primary dilated cardiomyopathy [RCV002524013]|not provided [RCV000493250] | likely benign|uncertain significance | 2 | 105363460 | 105363460 | Human | 1 | name |
| 13478901 | CV448423 | single nucleotide variant | NM_001318895.3(FHL2):c.576G>A (p.Arg192=) | Primary dilated cardiomyopathy [RCV000550274] | likely benign | 2 | 105363397 | 105363397 | Human | 1 | name |
| 13488407 | CV448597 | single nucleotide variant | NM_001318895.3(FHL2):c.351C>T (p.Tyr117=) | Primary dilated cardiomyopathy [RCV000532346] | likely benign | 2 | 105367720 | 105367720 | Human | 1 | name |
| 13533499 | CV496214 | single nucleotide variant | NM_001318895.3(FHL2):c.62T>A (p.Leu21Gln) | Primary dilated cardiomyopathy [RCV000799153]|not specified [RCV000607111] | uncertain significance | 2 | 105386455 | 105386455 | Human | 1 | name |
| 8611183 | CV57484 | single nucleotide variant | NM_001318895.3(FHL2):c.321C>T (p.Thr107=) | Cardiomyopathy [RCV000768817]|Primary dilated cardiomyopathy [RCV000463154]|not specified [RCV000041643] | benign|likely benign | 2 | 105373569 | 105373569 | Human | 3 | name |
| 8611185 | CV57486 | single nucleotide variant | NM_001318895.3(FHL2):c.462T>C (p.Tyr154=) | FHL2-related disorder [RCV003974926]|Primary dilated cardiomyopathy [RCV000557508]|not specified [RCV000041645] | likely benign | 2 | 105367609 | 105367609 | Human | 1 | name , trait , alternate_id |
| 8611187 | CV57488 | single nucleotide variant | NM_001318895.3(FHL2):c.678C>T (p.Asn226=) | Cardiomyopathy [RCV000768814]|FHL2-related disorder [RCV003915002]|Primary dilated cardiomyopathy [RCV000230608]|not provided [RCV004707900]|not specified [RCV000041647] | benign|uncertain significance | 2 | 105363295 | 105363295 | Human | 3 | name , trait , alternate_id |
| 8611192 | CV57493 | single nucleotide variant | NM_001318895.3(FHL2):c.804C>T (p.Asp268=) | Primary dilated cardiomyopathy [RCV001510993]|not provided [RCV001650879]|not specified [RCV000041652] | benign | 2 | 105361319 | 105361319 | Human | 3 | name |
| 8611192 | CV57493 | single nucleotide variant | NM_001318895.3(FHL2):c.804C>T (p.Asp268=) | Primary dilated cardiomyopathy [RCV001510993]|not provided [RCV001650879]|not specified [RCV000041652] | benign | 2 | 105361319 | 105361320 | Human | 3 | name |
| 8611193 | CV57494 | single nucleotide variant | NM_001318895.3(FHL2):c.819C>T (p.Pro273=) | Primary dilated cardiomyopathy [RCV001521362]|not provided [RCV001719781]|not specified [RCV000041653] | benign | 2 | 105361304 | 105361304 | Human | 1 | name |
| 8611194 | CV57495 | single nucleotide variant | NM_001318895.3(FHL2):c.85G>A (p.Val29Met) | Cardiomyopathy [RCV001171212]|FHL2-related disorder [RCV003934973]|Primary dilated cardiomyopathy [RCV000469953]|not specified [RCV000041654] | benign|likely benign|uncertain significance | 2 | 105386432 | 105386432 | Human | 3 | name , trait , alternate_id |
| 15156495 | CV685831 | single nucleotide variant | NM_001318895.3(FHL2):c.507C>T (p.Ile169=) | Primary dilated cardiomyopathy [RCV000868244] | likely benign | 2 | 105363466 | 105363466 | Human | 1 | name |
| 15202645 | CV762133 | single nucleotide variant | NM_001318895.3(FHL2):c.801G>A (p.Arg267=) | Primary dilated cardiomyopathy [RCV001480510] | likely benign | 2 | 105361322 | 105361322 | Human | 1 | name |
| 126754930 | CV1003114 | single nucleotide variant | NM_001318895.3(FHL2):c.121G>T (p.Glu41Ter) | Primary dilated cardiomyopathy [RCV001327622] | uncertain significance | 2 | 105386396 | 105386396 | Human | 1 | name |
| 126756125 | CV1023618 | deletion | NM_001318895.3(FHL2):c.533del (p.Glu178fs) | Primary dilated cardiomyopathy [RCV001339198] | uncertain significance | 2 | 105363440 | 105363440 | Human | 1 | name |
| 126754566 | CV1023620 | single nucleotide variant | NM_001318895.3(FHL2):c.175C>T (p.Arg59Trp) | Primary dilated cardiomyopathy [RCV001338849]|not specified [RCV004035872] | uncertain significance | 2 | 105373715 | 105373715 | Human | 1 | name |
| 126910210 | CV1040440 | single nucleotide variant | NM_001318895.3(FHL2):c.109G>A (p.Ala37Thr) | Primary dilated cardiomyopathy [RCV001365260] | uncertain significance | 2 | 105386408 | 105386408 | Human | 1 | name |
| 150555849 | CV1305341 | single nucleotide variant | NM_001318895.3(FHL2):c.164C>T (p.Ser55Phe) | not provided [RCV001773274] | uncertain significance | 2 | 105373726 | 105373726 | Human | | name |
| 151785254 | CV1342664 | duplication | NM_001318895.3(FHL2):c.337dup (p.Arg113fs) | Primary dilated cardiomyopathy [RCV002010117] | uncertain significance | 2 | 105367733 | 105367734 | Human | 1 | name |
| 151883127 | CV1384074 | single nucleotide variant | NM_001318895.3(FHL2):c.193T>C (p.Cys65Arg) | Primary dilated cardiomyopathy [RCV001886868] | uncertain significance | 2 | 105373697 | 105373697 | Human | 1 | name |
| 151742586 | CV1390902 | single nucleotide variant | NM_001318895.3(FHL2):c.224T>G (p.Leu75Arg) | Primary dilated cardiomyopathy [RCV001985382] | uncertain significance | 2 | 105373666 | 105373666 | Human | 1 | name |
| 151787261 | CV1416656 | single nucleotide variant | NM_001318895.3(FHL2):c.176G>A (p.Arg59Gln) | Primary dilated cardiomyopathy [RCV001989710] | uncertain significance | 2 | 105373714 | 105373714 | Human | 1 | name |
| 151725129 | CV1455616 | single nucleotide variant | NM_001318895.3(FHL2):c.219C>G (p.Asn73Lys) | Primary dilated cardiomyopathy [RCV002020684] | uncertain significance | 2 | 105373671 | 105373671 | Human | 1 | name |
| 151786817 | CV1495481 | single nucleotide variant | NM_001318895.3(FHL2):c.293C>T (p.Ser98Leu) | Primary dilated cardiomyopathy [RCV002026801]|not specified [RCV005343275] | uncertain significance | 2 | 105373597 | 105373597 | Human | 1 | name |
| 151794221 | CV1506078 | single nucleotide variant | NM_001318895.3(FHL2):c.211T>G (p.Cys71Gly) | Primary dilated cardiomyopathy [RCV001917111]|not specified [RCV004041174] | uncertain significance | 2 | 105373679 | 105373679 | Human | 1 | name |
| 151828276 | CV1510105 | single nucleotide variant | NM_001318895.3(FHL2):c.285C>G (p.Asn95Lys) | Primary dilated cardiomyopathy [RCV001920236] | uncertain significance | 2 | 105373605 | 105373605 | Human | 1 | name |
| 151874174 | CV1511436 | single nucleotide variant | NM_001318895.3(FHL2):c.125A>G (p.Glu42Gly) | Primary dilated cardiomyopathy [RCV001960835] | uncertain significance | 2 | 105386392 | 105386392 | Human | 1 | name |
| 9690924 | CV172933 | single nucleotide variant | NM_001318895.3(FHL2):c.284A>G (p.Asn95Ser) | not specified [RCV000156619] | uncertain significance | 2 | 105373606 | 105373606 | Human | | name |
| 9689253 | CV172935 | single nucleotide variant | NM_001318895.3(FHL2):c.109G>T (p.Ala37Ser) | Primary dilated cardiomyopathy [RCV000468337]|not provided [RCV004710562]|not specified [RCV000154723] | benign|likely benign | 2 | 105386408 | 105386408 | Human | 1 | name |
| 156374334 | CV1902042 | single nucleotide variant | NM_001318895.3(FHL2):c.191C>T (p.Ala64Val) | Primary dilated cardiomyopathy [RCV003092731] | uncertain significance | 2 | 105373699 | 105373699 | Human | 1 | name |
| 155933456 | CV1919884 | single nucleotide variant | NM_001318895.3(FHL2):c.269C>T (p.Thr90Ile) | Primary dilated cardiomyopathy [RCV002615136] | uncertain significance | 2 | 105373621 | 105373621 | Human | 1 | name |
| 156121307 | CV1924248 | single nucleotide variant | NM_001318895.3(FHL2):c.218A>G (p.Asn73Ser) | FHL2-related disorder [RCV003898897]|Primary dilated cardiomyopathy [RCV002640330] | uncertain significance | 2 | 105373672 | 105373672 | Human | 1 | name , trait , alternate_id |
| 156283660 | CV1929610 | single nucleotide variant | NM_001318895.3(FHL2):c.208C>G (p.Gln70Glu) | Primary dilated cardiomyopathy [RCV002628524] | uncertain significance | 2 | 105373682 | 105373682 | Human | 1 | name |
| 156014974 | CV2061555 | single nucleotide variant | NM_001318895.3(FHL2):c.162G>T (p.Leu54Phe) | Primary dilated cardiomyopathy [RCV002820327] | uncertain significance | 2 | 105373728 | 105373728 | Human | 1 | name |
| 11039966 | CV224221 | single nucleotide variant | NM_001318895.3(FHL2):c.236C>T (p.Pro79Leu) | not specified [RCV000208098] | uncertain significance | 2 | 105373654 | 105373654 | Human | | name |
| 156273373 | CV2293553 | single nucleotide variant | NM_001318895.3(FHL2):c.233A>G (p.Lys78Arg) | not specified [RCV004153078] | uncertain significance | 2 | 105373657 | 105373657 | Human | | name |
| 11348721 | CV238359 | single nucleotide variant | NM_001318895.3(FHL2):c.191C>G (p.Ala64Gly) | Primary dilated cardiomyopathy [RCV000227762] | likely pathogenic|uncertain significance | 2 | 105373699 | 105373699 | Human | 1 | name |
| 156392556 | CV2386478 | single nucleotide variant | NM_001318895.3(FHL2):c.245C>T (p.Ala82Val) | not specified [RCV004230844] | uncertain significance | 2 | 105373645 | 105373645 | Human | | name |
| 402523489 | CV2870086 | single nucleotide variant | NM_001318895.3(FHL2):c.254A>G (p.Asp85Gly) | Primary dilated cardiomyopathy [RCV003511023] | uncertain significance | 2 | 105373636 | 105373636 | Human | 1 | name |
| 402513611 | CV2925409 | single nucleotide variant | NM_001318895.3(FHL2):c.278A>T (p.Tyr93Phe) | Primary dilated cardiomyopathy [RCV003510201] | uncertain significance | 2 | 105373612 | 105373612 | Human | 1 | name |
| 405155153 | CV2971917 | single nucleotide variant | NM_001318895.3(FHL2):c.210G>T (p.Gln70His) | Primary dilated cardiomyopathy [RCV003620677] | uncertain significance | 2 | 105373680 | 105373680 | Human | 1 | name |
| 405158999 | CV2997977 | single nucleotide variant | NM_001318895.3(FHL2):c.154A>G (p.Lys52Glu) | Primary dilated cardiomyopathy [RCV003621004] | uncertain significance | 2 | 105386363 | 105386363 | Human | 1 | name |
| 405144604 | CV3046042 | single nucleotide variant | NM_001318895.3(FHL2):c.235C>G (p.Pro79Ala) | Primary dilated cardiomyopathy [RCV003619608] | uncertain significance | 2 | 105373655 | 105373655 | Human | 1 | name |
| 405779501 | CV3250531 | single nucleotide variant | NM_001318895.3(FHL2):c.259C>A (p.Leu87Met) | not specified [RCV004386404] | uncertain significance | 2 | 105373631 | 105373631 | Human | | name |
| 597752985 | CV3669493 | single nucleotide variant | NM_001318895.3(FHL2):c.284A>T (p.Asn95Ile) | not specified [RCV004924036] | uncertain significance | 2 | 105373606 | 105373606 | Human | | name |
| 597752990 | CV3669494 | single nucleotide variant | NM_001318895.3(FHL2):c.206C>T (p.Ser69Leu) | not specified [RCV004924037] | uncertain significance | 2 | 105373684 | 105373684 | Human | | name |
| 597872061 | CV3813872 | single nucleotide variant | NM_001318895.3(FHL2):c.236C>G (p.Pro79Arg) | Primary dilated cardiomyopathy [RCV005146940] | uncertain significance | 2 | 105373654 | 105373654 | Human | 1 | name |
| 597901973 | CV3835526 | deletion | NM_001318895.3(FHL2):c.780del (p.Arg261fs) | Primary dilated cardiomyopathy [RCV005176518] | uncertain significance | 2 | 105361343 | 105361343 | Human | 1 | name |
| 597901543 | CV3838856 | single nucleotide variant | NM_001318895.3(FHL2):c.266G>A (p.Cys89Tyr) | Primary dilated cardiomyopathy [RCV005176152] | uncertain significance | 2 | 105373624 | 105373624 | Human | 1 | name |
| 13485255 | CV448428 | single nucleotide variant | NM_001318895.3(FHL2):c.183G>T (p.Trp61Cys) | Primary dilated cardiomyopathy [RCV000553142] | uncertain significance | 2 | 105373707 | 105373707 | Human | 1 | name |
| 13465380 | CV448439 | single nucleotide variant | NM_001318895.3(FHL2):c.121G>A (p.Glu41Lys) | Primary dilated cardiomyopathy [RCV000542795] | uncertain significance | 2 | 105386396 | 105386396 | Human | 1 | name |
| 13541482 | CV496631 | single nucleotide variant | NM_001318895.3(FHL2):c.275G>A (p.Cys92Tyr) | Primary dilated cardiomyopathy [RCV002531672]|not specified [RCV000616222] | uncertain significance | 2 | 105373615 | 105373615 | Human | 1 | name |
| 13612271 | CV516253 | single nucleotide variant | NM_001318895.3(FHL2):c.130G>A (p.Gly44Arg) | Primary dilated cardiomyopathy [RCV000628801] | uncertain significance | 2 | 105386387 | 105386387 | Human | 1 | name |
| 14688781 | CV614741 | single nucleotide variant | NM_001318895.3(FHL2):c.142G>A (p.Gly48Ser) | Cardiomyopathy [RCV000769831]|FHL2-related disorder [RCV004756030]|Primary dilated cardiomyopathy [RCV000805165] | uncertain significance | 2 | 105386375 | 105386375 | Human | 3 | name , trait , alternate_id |
| 14709804 | CV628367 | single nucleotide variant | NM_001318895.3(FHL2):c.274T>C (p.Cys92Arg) | Primary dilated cardiomyopathy [RCV000809439] | uncertain significance | 2 | 105373616 | 105373616 | Human | 1 | name |
| 14714181 | CV628368 | single nucleotide variant | NM_001318895.3(FHL2):c.104T>G (p.Leu35Arg) | Primary dilated cardiomyopathy [RCV000794336] | uncertain significance | 2 | 105386413 | 105386413 | Human | 1 | name |
| 15015063 | CV679529 | single nucleotide variant | NM_001318895.3(FHL2):c.143G>A (p.Gly48Asp) | Primary dilated cardiomyopathy [RCV000853142] | uncertain significance | 2 | 105386374 | 105386374 | Human | 1 | name |
| 26905273 | CV824614 | single nucleotide variant | NM_001318895.3(FHL2):c.139A>G (p.Ile47Val) | Primary dilated cardiomyopathy [RCV001071765] | uncertain significance | 2 | 105386378 | 105386378 | Human | 1 | name |
| 38496256 | CV952599 | single nucleotide variant | NM_001318895.3(FHL2):c.128G>A (p.Cys43Tyr) | Primary dilated cardiomyopathy [RCV001242442] | uncertain significance | 2 | 105386389 | 105386389 | Human | 1 | name |
| 126739341 | CV987849 | single nucleotide variant | NM_001318895.3(FHL2):c.281C>T (p.Ser94Phe) | Primary dilated cardiomyopathy [RCV001305120] | uncertain significance | 2 | 105373609 | 105373609 | Human | 1 | name |
| 126740792 | CV1003112 | single nucleotide variant | NM_001318895.3(FHL2):c.388C>T (p.His130Tyr) | Primary dilated cardiomyopathy [RCV001314431] | uncertain significance | 2 | 105367683 | 105367683 | Human | 1 | name |
| 126772314 | CV1003113 | single nucleotide variant | NM_001318895.3(FHL2):c.338G>A (p.Arg113His) | Primary dilated cardiomyopathy [RCV001323679] | uncertain significance | 2 | 105367733 | 105367733 | Human | 1 | name |
| 126772802 | CV1023616 | single nucleotide variant | NM_001318895.3(FHL2):c.782G>A (p.Arg261His) | Primary dilated cardiomyopathy [RCV001345823]|not specified [RCV004036466] | uncertain significance | 2 | 105361341 | 105361341 | Human | 1 | name |
| 126770728 | CV1023617 | single nucleotide variant | NM_001318895.3(FHL2):c.559G>A (p.Val187Met) | Primary dilated cardiomyopathy [RCV001344636] | uncertain significance | 2 | 105363414 | 105363414 | Human | 1 | name |
| 126753910 | CV1023619 | single nucleotide variant | NM_001318895.3(FHL2):c.475G>A (p.Ala159Thr) | Primary dilated cardiomyopathy [RCV001338695] | uncertain significance | 2 | 105367596 | 105367596 | Human | 1 | name |
| 126910207 | CV1040439 | single nucleotide variant | NM_001318895.3(FHL2):c.568G>A (p.Ala190Thr) | Primary dilated cardiomyopathy [RCV001365220] | uncertain significance | 2 | 105363405 | 105363405 | Human | 1 | name |
| 151790114 | CV1377313 | single nucleotide variant | NM_001318895.3(FHL2):c.497A>G (p.Lys166Arg) | Primary dilated cardiomyopathy [RCV001898093] | uncertain significance | 2 | 105367574 | 105367574 | Human | 1 | name |
| 151814068 | CV1382920 | single nucleotide variant | NM_001318895.3(FHL2):c.742T>C (p.Cys248Arg) | Primary dilated cardiomyopathy [RCV002049133] | uncertain significance | 2 | 105361381 | 105361381 | Human | 1 | name |
| 151874182 | CV1470356 | single nucleotide variant | NM_001318895.3(FHL2):c.559G>T (p.Val187Leu) | Primary dilated cardiomyopathy [RCV001885651] | uncertain significance | 2 | 105363414 | 105363414 | Human | 1 | name |
| 151710134 | CV1487200 | single nucleotide variant | NM_001318895.3(FHL2):c.644A>C (p.Asp215Ala) | Primary dilated cardiomyopathy [RCV001889198] | uncertain significance | 2 | 105363329 | 105363329 | Human | 1 | name |
| 151732595 | CV1497634 | single nucleotide variant | NM_001318895.3(FHL2):c.731G>A (p.Trp244Ter) | Primary dilated cardiomyopathy [RCV001946209] | uncertain significance | 2 | 105361392 | 105361392 | Human | 1 | name |
| 9690564 | CV172790 | single nucleotide variant | NM_001318895.3(FHL2):c.678C>A (p.Asn226Lys) | Primary dilated cardiomyopathy [RCV001238155]|not specified [RCV000156246] | uncertain significance | 2 | 105363295 | 105363295 | Human | 1 | name |
| 9690194 | CV172791 | single nucleotide variant | NM_001318895.3(FHL2):c.595C>A (p.Arg199Ser) | Cardiomyopathy [RCV000768815]|not specified [RCV000155865] | uncertain significance | 2 | 105363378 | 105363378 | Human | 2 | name |
| 9689251 | CV172792 | single nucleotide variant | NM_001318895.3(FHL2):c.337C>T (p.Arg113Cys) | Cardiomyopathy [RCV001171209]|Primary dilated cardiomyopathy [RCV000546432]|not specified [RCV000154721] | likely benign|conflicting interpretations of pathogenicity|uncertain significance | 2 | 105367734 | 105367734 | Human | 3 | name |
| 9690724 | CV172931 | single nucleotide variant | NM_001318895.3(FHL2):c.671G>T (p.Cys224Phe) | not specified [RCV000156413] | uncertain significance | 2 | 105363302 | 105363302 | Human | | name |
| 9690269 | CV172932 | single nucleotide variant | NM_001318895.3(FHL2):c.512C>T (p.Thr171Met) | Primary dilated cardiomyopathy [RCV000535396]|not specified [RCV000155942] | uncertain significance | 2 | 105363461 | 105363461 | Human | 1 | name |
| 155689402 | CV1775077 | single nucleotide variant | NM_001318895.3(FHL2):c.729G>C (p.Gln243His) | Primary dilated cardiomyopathy [RCV002294806] | uncertain significance | 2 | 105361394 | 105361394 | Human | 1 | name |
| 9832368 | CV178471 | single nucleotide variant | NM_001318895.3(FHL2):c.823T>G (p.Cys275Gly) | Primary dilated cardiomyopathy [RCV000157238] | uncertain significance | 2 | 105361300 | 105361300 | Human | 1 | name |
| 156358281 | CV1873837 | single nucleotide variant | NM_001318895.3(FHL2):c.529C>T (p.Arg177Trp) | Primary dilated cardiomyopathy [RCV003065422] | uncertain significance | 2 | 105363444 | 105363444 | Human | 1 | name |
| 156051747 | CV1881645 | single nucleotide variant | NM_001318895.3(FHL2):c.462T>G (p.Tyr154Ter) | Primary dilated cardiomyopathy [RCV003078901]|not provided [RCV003491222] | uncertain significance | 2 | 105367609 | 105367609 | Human | 1 | name |
| 156027209 | CV2039660 | single nucleotide variant | NM_001318895.3(FHL2):c.760T>C (p.Cys254Arg) | Primary dilated cardiomyopathy [RCV002780951] | uncertain significance | 2 | 105361363 | 105361363 | Human | 1 | name |
| 155945117 | CV2062142 | single nucleotide variant | NM_001318895.3(FHL2):c.756G>T (p.Lys252Asn) | Primary dilated cardiomyopathy [RCV002815936] | uncertain significance | 2 | 105361367 | 105361367 | Human | 1 | name |
| 156182455 | CV2102519 | single nucleotide variant | NM_001318895.3(FHL2):c.805G>A (p.Asp269Asn) | Primary dilated cardiomyopathy [RCV002917185] | uncertain significance | 2 | 105361318 | 105361318 | Human | 1 | name |
| 11039977 | CV224218 | single nucleotide variant | NM_001318895.3(FHL2):c.815G>A (p.Cys272Tyr) | Left ventricular noncompaction cardiomyopathy [RCV000208122]|Primary dilated cardiomyopathy [RCV003509515] | uncertain significance | 2 | 105361308 | 105361308 | Human | 3 | name |
| 11040380 | CV224219 | single nucleotide variant | NM_001318895.3(FHL2):c.715T>G (p.Phe239Val) | Arrhythmogenic right ventricular cardiomyopathy [RCV000208406] | uncertain significance | 2 | 105361408 | 105361408 | Human | 1 | name |
| 11040064 | CV224220 | single nucleotide variant | NM_001318895.3(FHL2):c.340A>G (p.Lys114Glu) | Primary familial hypertrophic cardiomyopathy [RCV000208288] | uncertain significance | 2 | 105367731 | 105367731 | Human | 1 | name |
| 11088762 | CV228527 | single nucleotide variant | NM_001318895.3(FHL2):c.523A>C (p.Thr175Pro) | Primary dilated cardiomyopathy [RCV000463516]|not specified [RCV000213979] | uncertain significance | 2 | 105363450 | 105363450 | Human | 1 | name |
| 243062542 | CV2405015 | single nucleotide variant | NM_001318895.3(FHL2):c.752G>C (p.Cys251Ser) | Primary dilated cardiomyopathy [RCV003225261] | uncertain significance | 2 | 105361371 | 105361371 | Human | 1 | name |
| 329402921 | CV2462023 | single nucleotide variant | NM_001318895.3(FHL2):c.392G>T (p.Arg131Leu) | not specified [RCV004272203] | uncertain significance | 2 | 105367679 | 105367679 | Human | | name |
| 329377374 | CV2462580 | single nucleotide variant | NM_001318895.3(FHL2):c.548A>G (p.Lys183Arg) | not specified [RCV004278530] | likely benign | 2 | 105363425 | 105363425 | Human | | name |
| 402524608 | CV2888331 | single nucleotide variant | NM_001318895.3(FHL2):c.338G>T (p.Arg113Leu) | Primary dilated cardiomyopathy [RCV003511115] | uncertain significance | 2 | 105367733 | 105367733 | Human | 1 | name |
| 402505013 | CV2906246 | single nucleotide variant | NM_001318895.3(FHL2):c.794C>G (p.Thr265Arg) | Primary dilated cardiomyopathy [RCV003509171] | uncertain significance | 2 | 105361329 | 105361329 | Human | 1 | name |
| 402514414 | CV2925814 | single nucleotide variant | NM_001318895.3(FHL2):c.311G>A (p.Cys104Tyr) | Primary dilated cardiomyopathy [RCV003510249] | uncertain significance | 2 | 105373579 | 105373579 | Human | 1 | name |
| 405148221 | CV2954102 | single nucleotide variant | NM_001318895.3(FHL2):c.738C>G (p.Asn246Lys) | Primary dilated cardiomyopathy [RCV003620082] | uncertain significance | 2 | 105361385 | 105361385 | Human | 1 | name |
| 405157508 | CV2979048 | single nucleotide variant | NM_001318895.3(FHL2):c.574A>G (p.Arg192Gly) | Primary dilated cardiomyopathy [RCV003620884] | uncertain significance | 2 | 105363399 | 105363399 | Human | 1 | name |
| 405162724 | CV3016225 | single nucleotide variant | NM_001318895.3(FHL2):c.655A>C (p.Lys219Gln) | Primary dilated cardiomyopathy [RCV003621318] | uncertain significance | 2 | 105363318 | 105363318 | Human | 1 | name |
| 405120047 | CV3116405 | single nucleotide variant | NM_001318895.3(FHL2):c.596G>A (p.Arg199His) | Primary dilated cardiomyopathy [RCV003814706] | uncertain significance | 2 | 105363377 | 105363377 | Human | 1 | name |
| 405779489 | CV3250533 | single nucleotide variant | NM_001318895.3(FHL2):c.492G>C (p.Gln164His) | not specified [RCV004386406] | uncertain significance | 2 | 105367579 | 105367579 | Human | | name |
| 405779475 | CV3250535 | single nucleotide variant | NM_001318895.3(FHL2):c.584T>C (p.Leu195Pro) | not specified [RCV004386408] | uncertain significance | 2 | 105363389 | 105363389 | Human | | name |
| 407502433 | CV3435814 | single nucleotide variant | NM_001318895.3(FHL2):c.732G>T (p.Trp244Cys) | not specified [RCV004623458] | uncertain significance | 2 | 105361391 | 105361391 | Human | | name |
| 597752979 | CV3669492 | single nucleotide variant | NM_001318895.3(FHL2):c.640T>A (p.Cys214Ser) | not specified [RCV004924035] | uncertain significance | 2 | 105363333 | 105363333 | Human | | name |
| 597833671 | CV3760266 | single nucleotide variant | NM_001318895.3(FHL2):c.322A>C (p.Ile108Leu) | Primary dilated cardiomyopathy [RCV005085009] | uncertain significance | 2 | 105373568 | 105373568 | Human | 1 | name |
| 597844896 | CV3771791 | single nucleotide variant | NM_001318895.3(FHL2):c.629T>C (p.Leu210Pro) | Primary dilated cardiomyopathy [RCV005120317] | uncertain significance | 2 | 105363344 | 105363344 | Human | 1 | name |
| 597846845 | CV3771934 | single nucleotide variant | NM_001318895.3(FHL2):c.565A>C (p.Thr189Pro) | Primary dilated cardiomyopathy [RCV005122444] | uncertain significance | 2 | 105363408 | 105363408 | Human | 1 | name |
| 597868171 | CV3790811 | single nucleotide variant | NM_001318895.3(FHL2):c.536A>G (p.Gln179Arg) | Primary dilated cardiomyopathy [RCV005143026] | uncertain significance | 2 | 105363437 | 105363437 | Human | 1 | name |
| 597875945 | CV3804805 | single nucleotide variant | NM_001318895.3(FHL2):c.482A>T (p.Gln161Leu) | Primary dilated cardiomyopathy [RCV005151067] | uncertain significance | 2 | 105367589 | 105367589 | Human | 1 | name |
| 597876168 | CV3805054 | single nucleotide variant | NM_001318895.3(FHL2):c.485G>T (p.Cys162Phe) | Primary dilated cardiomyopathy [RCV005151316] | uncertain significance | 2 | 105367586 | 105367586 | Human | 1 | name |
| 597898056 | CV3827892 | single nucleotide variant | NM_001318895.3(FHL2):c.515G>A (p.Gly172Glu) | Primary dilated cardiomyopathy [RCV005172966] | uncertain significance | 2 | 105363458 | 105363458 | Human | 1 | name |
| 597918250 | CV3840884 | single nucleotide variant | NM_001318895.3(FHL2):c.805G>T (p.Asp269Tyr) | Primary dilated cardiomyopathy [RCV005193177] | uncertain significance | 2 | 105361318 | 105361318 | Human | 1 | name |
| 597909325 | CV3843110 | single nucleotide variant | NM_001318895.3(FHL2):c.808A>G (p.Ile270Val) | Primary dilated cardiomyopathy [RCV005184402] | uncertain significance | 2 | 105361315 | 105361315 | Human | 1 | name |
| 12891891 | CV391589 | single nucleotide variant | NM_001318895.3(FHL2):c.374C>A (p.Thr125Asn) | Primary dilated cardiomyopathy [RCV000477413] | uncertain significance | 2 | 105367697 | 105367697 | Human | 1 | name |
| 12906274 | CV414814 | single nucleotide variant | NM_001318895.3(FHL2):c.701C>T (p.Thr234Ile) | not provided [RCV000489026] | uncertain significance | 2 | 105361422 | 105361422 | Human | | name |
| 13472154 | CV448559 | single nucleotide variant | NM_001318895.3(FHL2):c.430A>G (p.Lys144Glu) | Primary dilated cardiomyopathy [RCV000547227] | uncertain significance | 2 | 105367641 | 105367641 | Human | 1 | name |
| 13536521 | CV496213 | single nucleotide variant | NM_001318895.3(FHL2):c.392G>A (p.Arg131His) | FHL2-related disorder [RCV003411448]|Primary dilated cardiomyopathy [RCV001036798]|not specified [RCV000609117] | likely benign|uncertain significance | 2 | 105367679 | 105367679 | Human | 1 | name , trait , alternate_id |
| 13813741 | CV557515 | single nucleotide variant | NM_001318895.3(FHL2):c.521T>C (p.Val174Ala) | Primary dilated cardiomyopathy [RCV000704591]|not specified [RCV005338330] | uncertain significance | 2 | 105363452 | 105363452 | Human | 1 | name |
| 13811403 | CV557517 | single nucleotide variant | NM_001318895.3(FHL2):c.509C>T (p.Thr170Ile) | Primary dilated cardiomyopathy [RCV000688731] | uncertain significance | 2 | 105363464 | 105363464 | Human | 1 | name |
| 13817218 | CV558665 | single nucleotide variant | NM_001318895.3(FHL2):c.610G>A (p.Asp204Asn) | Primary dilated cardiomyopathy [RCV000706871] | uncertain significance | 2 | 105363363 | 105363363 | Human | 1 | name |
| 13813147 | CV559168 | single nucleotide variant | NM_001318895.3(FHL2):c.402G>C (p.Gln134His) | FHL2-related disorder [RCV003945725]|Primary dilated cardiomyopathy [RCV000704166]|not specified [RCV004026654] | benign|likely benign|uncertain significance | 2 | 105367669 | 105367669 | Human | 1 | name , trait , alternate_id |
| 8611184 | CV57485 | single nucleotide variant | NM_001318895.3(FHL2):c.391C>T (p.Arg131Cys) | Primary dilated cardiomyopathy [RCV000703091]|not specified [RCV000041644] | uncertain significance | 2 | 105367680 | 105367680 | Human | 1 | name |
| 8611186 | CV57487 | single nucleotide variant | NM_001318895.3(FHL2):c.530G>A (p.Arg177Gln) | Cardiomyopathy [RCV000768816]|Primary dilated cardiomyopathy [RCV000205480]|not provided [RCV004707899]|not specified [RCV000041646] | benign | 2 | 105363443 | 105363443 | Human | 3 | name |
| 8611191 | CV57492 | single nucleotide variant | NM_001318895.3(FHL2):c.724C>T (p.Arg242Trp) | not specified [RCV000041651] | uncertain significance | 2 | 105361399 | 105361399 | Human | | name |
| 14711861 | CV628363 | single nucleotide variant | NM_001318895.3(FHL2):c.739G>A (p.Asp247Asn) | Primary dilated cardiomyopathy [RCV000793612] | uncertain significance | 2 | 105361384 | 105361384 | Human | 1 | name |
| 14720701 | CV628364 | single nucleotide variant | NM_001318895.3(FHL2):c.550G>A (p.Glu184Lys) | Primary dilated cardiomyopathy [RCV000796763] | uncertain significance | 2 | 105363423 | 105363423 | Human | 1 | name |
| 14732129 | CV628365 | single nucleotide variant | NM_001318895.3(FHL2):c.533A>C (p.Glu178Ala) | Primary dilated cardiomyopathy [RCV000818163] | uncertain significance | 2 | 105363440 | 105363440 | Human | 1 | name |
| 14703543 | CV628366 | single nucleotide variant | NM_001318895.3(FHL2):c.406A>G (p.Ile136Val) | Primary dilated cardiomyopathy [RCV000807421] | uncertain significance | 2 | 105367665 | 105367665 | Human | 1 | name |
| 26919612 | CV824612 | single nucleotide variant | NM_001318895.3(FHL2):c.721G>A (p.Glu241Lys) | Primary dilated cardiomyopathy [RCV001045969] | uncertain significance | 2 | 105361402 | 105361402 | Human | 1 | name |
| 26921641 | CV824613 | single nucleotide variant | NM_001318895.3(FHL2):c.688G>A (p.Gly230Arg) | Primary dilated cardiomyopathy [RCV001050417] | uncertain significance | 2 | 105363285 | 105363285 | Human | 1 | name |
| 28894918 | CV903742 | single nucleotide variant | NM_001318895.3(FHL2):c.725G>A (p.Arg242Gln) | Cardiomyopathy [RCV001170738]|Primary dilated cardiomyopathy [RCV001203093] | uncertain significance | 2 | 105361398 | 105361398 | Human | 3 | name |
| 38484496 | CV922204 | single nucleotide variant | NM_001318895.3(FHL2):c.820G>A (p.Asp274Asn) | Primary dilated cardiomyopathy [RCV001219457] | uncertain significance | 2 | 105361303 | 105361303 | Human | 1 | name |
| 38489040 | CV930745 | single nucleotide variant | NM_001318895.3(FHL2):c.521T>A (p.Val174Asp) | Primary dilated cardiomyopathy [RCV001210028]|not specified [RCV004033786] | uncertain significance | 2 | 105363452 | 105363452 | Human | 1 | name |
| 38483149 | CV942175 | single nucleotide variant | NM_001318895.3(FHL2):c.595C>T (p.Arg199Cys) | Primary dilated cardiomyopathy [RCV001235807] | uncertain significance | 2 | 105363378 | 105363378 | Human | 1 | name |
| 38481088 | CV942176 | single nucleotide variant | NM_001318895.3(FHL2):c.307G>A (p.Glu103Lys) | Primary dilated cardiomyopathy [RCV001234966] | uncertain significance | 2 | 105373583 | 105373583 | Human | 1 | name |
| 126758183 | CV987848 | single nucleotide variant | NM_001318895.3(FHL2):c.487G>A (p.Val163Ile) | Primary dilated cardiomyopathy [RCV001299113]|not specified [RCV004619605] | uncertain significance | 2 | 105367584 | 105367584 | Human | 1 | name |
| 405159053 | CV2998219 | deletion | NM_001318895.3(FHL2):c.566_593del (p.Thr189fs) | Primary dilated cardiomyopathy [RCV003621008] | uncertain significance | 2 | 105363380 | 105363407 | Human | 1 | name |
| 156066940 | CV1888850 | indel | NM_001318895.3(FHL2):c.698_699delinsAA (p.Gly233Glu) | Primary dilated cardiomyopathy [RCV003079409] | uncertain significance | 2 | 105361424 | 105361425 | Human | | name |
| 402517327 | CV2865619 | deletion | NM_001318895.3(FHL2):c.235_249del (p.Pro79_Lys83del) | Primary dilated cardiomyopathy [RCV003510522] | uncertain significance | 2 | 105373641 | 105373655 | Human | 1 | name |
