| 597957525 | CV3814382 | single nucleotide variant | NM_198391.3(FLRT3):c.9C>T (p.Ser3=) | not provided [RCV005162713] | likely benign | 20 | 14327498 | 14327498 | Human | | name |
| 15116005 | CV786326 | single nucleotide variant | NM_198391.3(FLRT3):c.90C>A (p.Ser30=) | not provided [RCV000978513] | likely benign | 20 | 14327417 | 14327417 | Human | | name |
| 156354156 | CV2154068 | single nucleotide variant | NM_198391.3(FLRT3):c.189C>A (p.Leu63=) | not provided [RCV003031102] | likely benign | 20 | 14327318 | 14327318 | Human | | name |
| 156076075 | CV2291475 | single nucleotide variant | NM_198391.3(FLRT3):c.14C>T (p.Ala5Val) | not specified [RCV004155795] | uncertain significance | 20 | 14327493 | 14327493 | Human | | name |
| 597963403 | CV3841438 | single nucleotide variant | NM_198391.3(FLRT3):c.10G>A (p.Ala4Thr) | not provided [RCV005193542] | uncertain significance | 20 | 14327497 | 14327497 | Human | | name |
| 156240196 | CV2188823 | single nucleotide variant | NM_198391.3(FLRT3):c.447A>G (p.Ala149=) | not provided [RCV003059629] | likely benign | 20 | 14327060 | 14327060 | Human | | name |
| 401861757 | CV2756485 | single nucleotide variant | NM_198391.3(FLRT3):c.73T>C (p.Ser25Pro) | not specified [RCV004343016] | uncertain significance | 20 | 14327434 | 14327434 | Human | | name |
| 401924564 | CV2804954 | single nucleotide variant | NM_198391.3(FLRT3):c.741A>T (p.Thr247=) | not specified [RCV003404773] | likely benign | 20 | 14326766 | 14326766 | Human | | name |
| 401919631 | CV2827103 | single nucleotide variant | NM_198391.3(FLRT3):c.363T>C (p.Tyr121=) | FLRT3-related disorder [RCV003946591]|not provided [RCV003431259] | likely benign | 20 | 14327144 | 14327144 | Human | 1 | name , trait , alternate_id |
| 402474727 | CV3182803 | single nucleotide variant | NM_198391.3(FLRT3):c.414C>T (p.Asn138=) | not provided [RCV003875047] | likely benign | 20 | 14327093 | 14327093 | Human | | name |
| 405727086 | CV3257150 | single nucleotide variant | NM_198391.3(FLRT3):c.80T>C (p.Met27Thr) | not specified [RCV004389508] | uncertain significance | 20 | 14327427 | 14327427 | Human | | name |
| 597831705 | CV3740071 | single nucleotide variant | NM_198391.3(FLRT3):c.963A>G (p.Gln321=) | not provided [RCV005062769] | likely benign | 20 | 14326544 | 14326544 | Human | | name |
| 597872757 | CV3849553 | single nucleotide variant | NM_198391.3(FLRT3):c.897A>G (p.Gln299=) | not provided [RCV005197734] | likely benign | 20 | 14326610 | 14326610 | Human | | name |
| 598201999 | CV3977099 | single nucleotide variant | NM_198391.3(FLRT3):c.58C>A (p.Gln20Lys) | not specified [RCV005337005] | uncertain significance | 20 | 14327449 | 14327449 | Human | | name |
| 15169320 | CV705385 | single nucleotide variant | NM_198391.3(FLRT3):c.765A>G (p.Gln255=) | not provided [RCV000949434] | benign|likely benign | 20 | 14326742 | 14326742 | Human | | name |
| 15166377 | CV716861 | single nucleotide variant | NM_198391.3(FLRT3):c.948A>T (p.Val316=) | not provided [RCV000971165] | likely benign | 20 | 14326559 | 14326559 | Human | | name |
| 15171395 | CV716862 | single nucleotide variant | NM_198391.3(FLRT3):c.831T>C (p.Asp277=) | not provided [RCV000972191] | benign | 20 | 14326676 | 14326676 | Human | | name |
| 15152079 | CV757384 | single nucleotide variant | NM_198391.3(FLRT3):c.738C>A (p.Gly246=) | not provided [RCV000923802] | likely benign | 20 | 14326769 | 14326769 | Human | | name |
| 15135301 | CV773008 | single nucleotide variant | NM_198391.3(FLRT3):c.936G>A (p.Lys312=) | not provided [RCV000942897] | likely benign | 20 | 14326571 | 14326571 | Human | | name |
| 15174881 | CV773009 | single nucleotide variant | NM_198391.3(FLRT3):c.591T>G (p.Gly197=) | not provided [RCV000928542] | benign | 20 | 14326916 | 14326916 | Human | | name |
| 150404899 | CV1189409 | single nucleotide variant | NM_198391.3(FLRT3):c.182C>G (p.Thr61Arg) | Disorder of sexual differentiation [RCV001564037] | uncertain significance | 20 | 14327325 | 14327325 | Human | 1 | name |
| 150433538 | CV1216943 | single nucleotide variant | NM_198391.3(FLRT3):c.1257C>T (p.Thr419=) | Hypogonadotropic hypogonadism 21 with or without anosmia [RCV001702932]|not provided [RCV001608845] | benign | 20 | 14326250 | 14326250 | Human | 1 | name |
| 405269549 | CV3201714 | single nucleotide variant | NM_198391.3(FLRT3):c.1327C>T (p.Leu443=) | FLRT3-related disorder [RCV003899621] | likely benign | 20 | 14326180 | 14326180 | Human | | name , trait , alternate_id |
| 405727079 | CV3257149 | single nucleotide variant | NM_198391.3(FLRT3):c.218C>A (p.Ala73Asp) | not specified [RCV004389507] | uncertain significance | 20 | 14327289 | 14327289 | Human | | name |
| 597934677 | CV3810977 | duplication | NM_198391.3(FLRT3):c.132dup (p.Asn45Ter) | not provided [RCV005157686] | uncertain significance | 20 | 14327374 | 14327375 | Human | | name |
| 8611971 | CV59848 | single nucleotide variant | NM_198391.3(FLRT3):c.290A>G (p.Glu97Gly) | HYPOGONADOTROPIC HYPOGONADISM 21 WITH ANOSMIA, SUSCEPTIBILITY TO [RCV000043602] | risk factor | 20 | 14327217 | 14327217 | Human | | name |
| 8611973 | CV59850 | single nucleotide variant | NM_198391.3(FLRT3):c.205C>A (p.Gln69Lys) | HYPOGONADOTROPIC HYPOGONADISM 21 WITH ANOSMIA, SUSCEPTIBILITY TO [RCV000043604] | risk factor | 20 | 14327302 | 14327302 | Human | | name |
| 15152698 | CV716860 | single nucleotide variant | NM_198391.3(FLRT3):c.1104T>C (p.Thr368=) | not provided [RCV000968403] | benign | 20 | 14326403 | 14326403 | Human | | name |
| 15193838 | CV757383 | single nucleotide variant | NM_198391.3(FLRT3):c.1323T>C (p.Leu441=) | not provided [RCV000910952]|not specified [RCV005236429] | benign|likely benign | 20 | 14326184 | 14326184 | Human | | name |
| 151764573 | CV1387342 | single nucleotide variant | NM_198391.3(FLRT3):c.700C>T (p.Arg234Trp) | not provided [RCV001987647] | uncertain significance | 20 | 14326807 | 14326807 | Human | | name |
| 151858945 | CV1389508 | single nucleotide variant | NM_198391.3(FLRT3):c.452G>A (p.Arg151Gln) | not provided [RCV001905036] | uncertain significance | 20 | 14327055 | 14327055 | Human | | name |
| 151881946 | CV1402332 | single nucleotide variant | NM_198391.3(FLRT3):c.821A>G (p.Tyr274Cys) | not provided [RCV001961823] | uncertain significance | 20 | 14326686 | 14326686 | Human | | name |
| 155644091 | CV1708416 | single nucleotide variant | NM_198391.3(FLRT3):c.999G>A (p.Met333Ile) | Hypogonadotropic hypogonadism 21 with or without anosmia [RCV002290405] | uncertain significance | 20 | 14326508 | 14326508 | Human | 1 | name |
| 156263847 | CV2128889 | single nucleotide variant | NM_198391.3(FLRT3):c.950G>A (p.Arg317His) | FLRT3-related disorder [RCV003961286]|not provided [RCV002933981] | likely benign | 20 | 14326557 | 14326557 | Human | 1 | name , trait , alternate_id |
| 156080043 | CV2226593 | single nucleotide variant | NM_198391.3(FLRT3):c.907C>T (p.Arg303Cys) | not specified [RCV004101843] | uncertain significance | 20 | 14326600 | 14326600 | Human | | name |
| 156254061 | CV2264621 | single nucleotide variant | NM_198391.3(FLRT3):c.985G>A (p.Val329Met) | not specified [RCV004132627] | uncertain significance | 20 | 14326522 | 14326522 | Human | | name |
| 156003620 | CV2295715 | single nucleotide variant | NM_198391.3(FLRT3):c.977A>G (p.Lys326Arg) | not specified [RCV004149863] | uncertain significance | 20 | 14326530 | 14326530 | Human | | name |
| 401717955 | CV2725163 | single nucleotide variant | NM_198391.3(FLRT3):c.487C>T (p.Arg163Cys) | not specified [RCV004319903] | uncertain significance | 20 | 14327020 | 14327020 | Human | | name |
| 401878722 | CV2777016 | single nucleotide variant | NM_198391.3(FLRT3):c.299C>T (p.Thr100Ile) | not specified [RCV004351815] | uncertain significance | 20 | 14327208 | 14327208 | Human | | name |
| 405071169 | CV2876543 | single nucleotide variant | NM_198391.3(FLRT3):c.943T>A (p.Trp315Arg) | not provided [RCV003548541] | uncertain significance | 20 | 14326564 | 14326564 | Human | | name |
| 405217643 | CV3143745 | single nucleotide variant | NM_198391.3(FLRT3):c.526A>T (p.Thr176Ser) | not provided [RCV003846715] | uncertain significance | 20 | 14326981 | 14326981 | Human | | name |
| 405259491 | CV3186292 | single nucleotide variant | NM_198391.3(FLRT3):c.992G>A (p.Gly331Glu) | not provided [RCV003884051] | uncertain significance | 20 | 14326515 | 14326515 | Human | | name |
| 407479350 | CV3432347 | single nucleotide variant | NM_198391.3(FLRT3):c.812G>A (p.Arg271Lys) | not specified [RCV004625867] | uncertain significance | 20 | 14326695 | 14326695 | Human | | name |
| 407479359 | CV3432349 | single nucleotide variant | NM_198391.3(FLRT3):c.852T>A (p.Ser284Arg) | not provided [RCV005059656]|not specified [RCV004625869] | uncertain significance | 20 | 14326655 | 14326655 | Human | | name |
| 407479361 | CV3432350 | single nucleotide variant | NM_198391.3(FLRT3):c.908G>A (p.Arg303His) | not specified [RCV004625870] | uncertain significance | 20 | 14326599 | 14326599 | Human | | name |
| 408367248 | CV3518055 | single nucleotide variant | NM_198391.3(FLRT3):c.596C>G (p.Thr199Ser) | FLRT3-related disorder [RCV004757944] | uncertain significance | 20 | 14326911 | 14326911 | Human | | name , trait , alternate_id |
| 597883215 | CV3784220 | single nucleotide variant | NM_198391.3(FLRT3):c.718G>A (p.Ala240Thr) | not provided [RCV005124509] | uncertain significance | 20 | 14326789 | 14326789 | Human | | name |
| 8611972 | CV59849 | single nucleotide variant | NM_198391.3(FLRT3):c.431G>T (p.Ser144Ile) | HYPOGONADOTROPIC HYPOGONADISM 21 WITH ANOSMIA, SUSCEPTIBILITY TO [RCV000043603] | risk factor | 20 | 14327076 | 14327076 | Human | | name |
| 126744510 | CV1018666 | single nucleotide variant | NM_198391.3(FLRT3):c.1255A>T (p.Thr419Ser) | Hypogonadotropic hypogonadism 21 with or without anosmia [RCV001330454]|not provided [RCV002546391] | uncertain significance | 20 | 14326252 | 14326252 | Human | 1 | name |
| 150485672 | CV1250278 | single nucleotide variant | NM_198391.3(FLRT3):c.1380A>C (p.Glu460Asp) | not provided [RCV001673891] | benign | 20 | 14326127 | 14326127 | Human | | name |
| 150455906 | CV1278422 | single nucleotide variant | NM_198391.3(FLRT3):c.1200C>A (p.His400Gln) | not provided [RCV001709037] | benign | 20 | 14326307 | 14326307 | Human | | name |
| 150553836 | CV1306653 | single nucleotide variant | NM_198391.3(FLRT3):c.1134A>C (p.Gln378His) | not provided [RCV001769717] | benign|likely benign | 20 | 14326373 | 14326373 | Human | | name |
| 151733326 | CV1336537 | single nucleotide variant | NM_198391.3(FLRT3):c.1202A>T (p.Gln401Leu) | Amenorrhea [RCV001849766] | uncertain significance | 20 | 14326305 | 14326305 | Human | 2 | name |
| 152041848 | CV1669924 | single nucleotide variant | NM_198391.3(FLRT3):c.1354A>G (p.Ile452Val) | not provided [RCV002224826] | uncertain significance | 20 | 14326153 | 14326153 | Human | | name |
| 156305955 | CV1868188 | single nucleotide variant | NM_198391.3(FLRT3):c.1382G>A (p.Arg461His) | not provided [RCV003062189] | uncertain significance | 20 | 14326125 | 14326125 | Human | | name |
| 156369790 | CV2190660 | single nucleotide variant | NM_198391.3(FLRT3):c.1112C>T (p.Pro371Leu) | not provided [RCV003066197] | uncertain significance | 20 | 14326395 | 14326395 | Human | | name |
| 155987252 | CV2248067 | single nucleotide variant | NM_198391.3(FLRT3):c.1445T>A (p.Met482Lys) | not specified [RCV004115346] | uncertain significance | 20 | 14326062 | 14326062 | Human | | name |
| 156275664 | CV2316476 | single nucleotide variant | NM_198391.3(FLRT3):c.1792C>T (p.Pro598Ser) | not specified [RCV004169955] | uncertain significance | 20 | 14325715 | 14325715 | Human | | name |
| 11350751 | CV236926 | single nucleotide variant | NM_198391.3(FLRT3):c.1129G>A (p.Ala377Thr) | not provided [RCV000224340] | benign|likely benign | 20 | 14326378 | 14326378 | Human | | name |
| 243053336 | CV2410174 | single nucleotide variant | NM_198391.3(FLRT3):c.1727C>T (p.Ala576Val) | Hypogonadotropic hypogonadism 21 with or without anosmia [RCV003144060] | uncertain significance | 20 | 14325780 | 14325780 | Human | 1 | name |
| 329361353 | CV2436927 | single nucleotide variant | NM_198391.3(FLRT3):c.1604G>T (p.Gly535Val) | not specified [RCV004260308] | uncertain significance | 20 | 14325903 | 14325903 | Human | | name |
| 401736107 | CV2672824 | single nucleotide variant | NM_198391.3(FLRT3):c.1396G>C (p.Val466Leu) | FLRT3-related disorder [RCV003900995]|not provided [RCV005256911]|not specified [RCV004281601] | likely benign|uncertain significance | 20 | 14326111 | 14326111 | Human | 1 | name , trait , alternate_id |
| 401752495 | CV2707028 | single nucleotide variant | NM_198391.3(FLRT3):c.1510C>T (p.Leu504Phe) | not specified [RCV004321621] | uncertain significance | 20 | 14325997 | 14325997 | Human | | name |
| 405144227 | CV3126139 | single nucleotide variant | NM_198391.3(FLRT3):c.1907A>G (p.Tyr636Cys) | not provided [RCV003817055] | uncertain significance | 20 | 14325600 | 14325600 | Human | | name |
| 405138920 | CV3130839 | single nucleotide variant | NM_198391.3(FLRT3):c.1018G>T (p.Val340Phe) | not provided [RCV003839073] | uncertain significance | 20 | 14326489 | 14326489 | Human | | name |
| 405727053 | CV3257146 | single nucleotide variant | NM_198391.3(FLRT3):c.1339C>G (p.Pro447Ala) | not specified [RCV004389504] | uncertain significance | 20 | 14326168 | 14326168 | Human | | name |
| 405727062 | CV3257147 | single nucleotide variant | NM_198391.3(FLRT3):c.1865T>C (p.Leu622Pro) | not specified [RCV004389505] | uncertain significance | 20 | 14325642 | 14325642 | Human | | name |
| 405727069 | CV3257148 | single nucleotide variant | NM_198391.3(FLRT3):c.1906T>C (p.Tyr636His) | not specified [RCV004389506] | uncertain significance | 20 | 14325601 | 14325601 | Human | | name |
| 407479346 | CV3432346 | single nucleotide variant | NM_198391.3(FLRT3):c.1814C>T (p.Ser605Leu) | not specified [RCV004625866] | uncertain significance | 20 | 14325693 | 14325693 | Human | | name |
| 407479354 | CV3432348 | single nucleotide variant | NM_198391.3(FLRT3):c.1705A>G (p.Arg569Gly) | not specified [RCV004625868] | uncertain significance | 20 | 14325802 | 14325802 | Human | | name |
| 407479366 | CV3432351 | single nucleotide variant | NM_198391.3(FLRT3):c.1216C>T (p.Pro406Ser) | not specified [RCV004625871] | uncertain significance | 20 | 14326291 | 14326291 | Human | | name |
| 597700952 | CV3676380 | single nucleotide variant | NM_198391.3(FLRT3):c.1388A>G (p.Glu463Gly) | not specified [RCV004916393] | uncertain significance | 20 | 14326119 | 14326119 | Human | | name |
| 597838418 | CV3736898 | single nucleotide variant | NM_198391.3(FLRT3):c.1535C>T (p.Thr512Ile) | not provided [RCV005064378] | uncertain significance | 20 | 14325972 | 14325972 | Human | | name |
| 597956823 | CV3838321 | single nucleotide variant | NM_198391.3(FLRT3):c.1343C>T (p.Ala448Val) | not provided [RCV005191696] | uncertain significance | 20 | 14326164 | 14326164 | Human | | name |
| 597917280 | CV3861337 | single nucleotide variant | NM_198391.3(FLRT3):c.1319G>A (p.Trp440Ter) | not provided [RCV005204494] | uncertain significance | 20 | 14326188 | 14326188 | Human | | name |
| 598176954 | CV4008216 | single nucleotide variant | NM_198391.3(FLRT3):c.1166C>T (p.Pro389Leu) | Hypogonadotropic hypogonadism 21 with or without anosmia [RCV005393732] | uncertain significance | 20 | 14326341 | 14326341 | Human | 1 | name |
| 616934103 | CV4012103 | single nucleotide variant | NM_198391.3(FLRT3):c.1141T>C (p.Trp381Arg) | not specified [RCV005409137] | uncertain significance | 20 | 14326366 | 14326366 | Human | | name |
| 617153357 | CV4018566 | single nucleotide variant | NM_198391.3(FLRT3):c.1802A>G (p.Asn601Ser) | not specified [RCV005418828] | uncertain significance | 20 | 14325705 | 14325705 | Human | | name |
| 8611974 | CV59851 | single nucleotide variant | NM_198391.3(FLRT3):c.1016A>G (p.Lys339Arg) | Hypogonadotropic hypogonadism 21 with or without anosmia [RCV000043605] | pathogenic | 20 | 14326491 | 14326491 | Human | 1 | name |
| 14696169 | CV612419 | single nucleotide variant | NM_198391.3(FLRT3):c.1642G>C (p.Val548Leu) | High myopia [RCV000785716] | uncertain significance | 20 | 14325865 | 14325865 | Human | 2 | name |
| 38466443 | CV920967 | single nucleotide variant | NM_198391.3(FLRT3):c.1829T>C (p.Val610Ala) | not provided [RCV001200147] | uncertain significance | 20 | 14325678 | 14325678 | Human | | name |
