| 152166810 | CV1666403 | single nucleotide variant | NM_001136219.3(FCGR2A):c.780+1G>A | Cystic fibrosis [RCV002204527]|not provided [RCV004691491] | uncertain significance | 1 | 161513933 | 161513933 | Human | 2 | name |
| 617151488 | CV4022005 | single nucleotide variant | NM_001136219.3(FCGR2A):c.619+6G>C | not provided [RCV005426966] | likely benign | 1 | 161510080 | 161510080 | Human | | name |
| 12896944 | CV389316 | single nucleotide variant | NM_001136219.3(FCGR2A):c.365-11G>A | not provided [RCV004714000]|not specified [RCV000456031] | benign | 1 | 161509809 | 161509809 | Human | | name |
| 405276726 | CV3193465 | single nucleotide variant | NM_001136219.3(FCGR2A):c.153C>T (p.Asn51=) | FCGR2A-related disorder [RCV003974633] | likely benign | 1 | 161506380 | 161506380 | Human | | name , trait , alternate_id |
| 405272794 | CV3210147 | single nucleotide variant | NM_001136219.3(FCGR2A):c.144G>A (p.Pro48=) | FCGR2A-related disorder [RCV003914393] | likely benign | 1 | 161506371 | 161506371 | Human | | name , trait , alternate_id |
| 407482874 | CV3438825 | single nucleotide variant | NM_001136219.3(FCGR2A):c.22T>C (p.Ser8Pro) | not specified [RCV004618469] | uncertain significance | 1 | 161505489 | 161505489 | Human | | name |
| 15187721 | CV718332 | single nucleotide variant | NM_001136219.3(FCGR2A):c.210C>T (p.Ser70=) | not provided [RCV000887332] | benign|likely benign | 1 | 161506437 | 161506437 | Human | | name |
| 150492936 | CV1274839 | single nucleotide variant | NM_001136219.3(FCGR2A):c.363C>T (p.Ser121=) | not provided [RCV001702143] | likely benign | 1 | 161506590 | 161506590 | Human | | name |
| 12896897 | CV389342 | single nucleotide variant | NM_001136219.3(FCGR2A):c.879C>T (p.Pro293=) | not provided [RCV004714001]|not specified [RCV000455964] | benign | 1 | 161518073 | 161518073 | Human | | name |
| 12896616 | CV389346 | single nucleotide variant | NM_001136219.3(FCGR2A):c.645A>G (p.Pro215=) | not provided [RCV004715201]|not specified [RCV000455589] | benign | 1 | 161510859 | 161510859 | Human | | name |
| 598229290 | CV3959082 | single nucleotide variant | NM_001136219.3(FCGR2A):c.75G>T (p.Leu25Phe) | not specified [RCV005342049] | uncertain significance | 1 | 161505542 | 161505542 | Human | | name |
| 156386980 | CV2221368 | single nucleotide variant | NM_001136219.3(FCGR2A):c.281C>T (p.Ala94Val) | not specified [RCV004096671] | uncertain significance | 1 | 161506508 | 161506508 | Human | | name |
| 156239862 | CV2286004 | single nucleotide variant | NM_001136219.3(FCGR2A):c.221A>C (p.Gln74Pro) | not specified [RCV004143913] | uncertain significance | 1 | 161506448 | 161506448 | Human | | name |
| 405725629 | CV3256795 | single nucleotide variant | NM_001136219.3(FCGR2A):c.257C>T (p.Thr86Met) | not specified [RCV004389340] | uncertain significance | 1 | 161506484 | 161506484 | Human | | name |
| 12896455 | CV389336 | single nucleotide variant | NM_001136219.3(FCGR2A):c.187C>T (p.Gln63Ter) | FCGR2A-related disorder [RCV003972704]|not provided [RCV004713999]|not specified [RCV000455363] | benign | 1 | 161506414 | 161506414 | Human | 6 | name , trait , alternate_id |
| 12896455 | CV389336 | single nucleotide variant | NM_001136219.3(FCGR2A):c.187C>T (p.Gln63Ter) | FCGR2A-related disorder [RCV003972704]|not provided [RCV004713999]|not specified [RCV000455363] | benign | 1 | 161506414 | 161506415 | Human | 6 | name , trait , alternate_id |
| 12896942 | CV389339 | single nucleotide variant | NM_001136219.3(FCGR2A):c.188A>G (p.Gln63Arg) | FCGR2A-related disorder [RCV003970260]|not provided [RCV004713998]|not specified [RCV000456029] | benign | 1 | 161506415 | 161506415 | Human | 4 | name , trait , alternate_id |
| 12896942 | CV389339 | single nucleotide variant | NM_001136219.3(FCGR2A):c.188A>G (p.Gln63Arg) | FCGR2A-related disorder [RCV003970260]|not provided [RCV004713998]|not specified [RCV000456029] | benign | 1 | 161506415 | 161506416 | Human | 4 | name , trait , alternate_id |
| 598229273 | CV3959077 | single nucleotide variant | NM_001136219.3(FCGR2A):c.218T>G (p.Ile73Ser) | not specified [RCV005342046] | uncertain significance | 1 | 161506445 | 161506445 | Human | | name |
| 598229285 | CV3959079 | single nucleotide variant | NM_001136219.3(FCGR2A):c.247C>G (p.Pro83Ala) | not specified [RCV005342048] | uncertain significance | 1 | 161506474 | 161506474 | Human | | name |
| 598271877 | CV3959081 | single nucleotide variant | NM_001136219.3(FCGR2A):c.119A>G (p.Lys40Arg) | not specified [RCV005327840] | uncertain significance | 1 | 161506346 | 161506346 | Human | | name |
| 150435758 | CV1274885 | single nucleotide variant | NM_001136219.3(FCGR2A):c.418A>G (p.Met140Val) | not provided [RCV001702155] | likely benign | 1 | 161509873 | 161509873 | Human | | name |
| 152061720 | CV1666402 | single nucleotide variant | NM_001136219.3(FCGR2A):c.497C>T (p.Ser166Phe) | Cystic fibrosis [RCV002208746] | uncertain significance | 1 | 161509952 | 161509952 | Human | 2 | name |
| 156187725 | CV2195799 | single nucleotide variant | NM_001136219.3(FCGR2A):c.776T>C (p.Phe259Ser) | not specified [RCV004076148] | uncertain significance | 1 | 161513928 | 161513928 | Human | | name |
| 156380114 | CV2211790 | single nucleotide variant | NM_001136219.3(FCGR2A):c.671T>C (p.Ile224Thr) | not specified [RCV004086625] | likely benign | 1 | 161510885 | 161510885 | Human | | name |
| 156380119 | CV2211791 | single nucleotide variant | NM_001136219.3(FCGR2A):c.674C>G (p.Ala225Gly) | not specified [RCV004086626] | likely benign | 1 | 161510888 | 161510888 | Human | | name |
| 156380124 | CV2211792 | single nucleotide variant | NM_001136219.3(FCGR2A):c.677C>T (p.Thr226Ile) | not specified [RCV004086627] | likely benign | 1 | 161510891 | 161510891 | Human | | name |
| 156306132 | CV2314842 | single nucleotide variant | NM_001136219.3(FCGR2A):c.514T>C (p.Phe172Leu) | not specified [RCV004170961] | uncertain significance | 1 | 161509969 | 161509969 | Human | | name |
| 156185112 | CV2377804 | single nucleotide variant | NM_001136219.3(FCGR2A):c.895G>A (p.Asp299Asn) | not specified [RCV004230384] | uncertain significance | 1 | 161518089 | 161518089 | Human | | name |
| 156097161 | CV2399170 | single nucleotide variant | NM_001136219.3(FCGR2A):c.614T>C (p.Val205Ala) | not specified [RCV004246601] | uncertain significance | 1 | 161510069 | 161510069 | Human | | name |
| 329387618 | CV2446726 | single nucleotide variant | NM_001136219.3(FCGR2A):c.734G>A (p.Arg245Gln) | not specified [RCV004253767] | likely benign | 1 | 161510948 | 161510948 | Human | | name |
| 329385231 | CV2451112 | single nucleotide variant | NM_001136219.3(FCGR2A):c.449C>G (p.Pro150Arg) | not specified [RCV004270051] | uncertain significance | 1 | 161509904 | 161509904 | Human | | name |
| 401725265 | CV2726086 | single nucleotide variant | NM_001136219.3(FCGR2A):c.626G>C (p.Ser209Thr) | not specified [RCV004324439] | uncertain significance | 1 | 161510840 | 161510840 | Human | | name |
| 401859154 | CV2771430 | single nucleotide variant | NM_001136219.3(FCGR2A):c.635G>A (p.Ser212Asn) | not specified [RCV004348480] | uncertain significance | 1 | 161510849 | 161510849 | Human | | name |
| 401933113 | CV2806119 | single nucleotide variant | NM_001136219.3(FCGR2A):c.648G>A (p.Met216Ile) | not provided [RCV003409205] | likely benign | 1 | 161510862 | 161510862 | Human | | name |
| 401942869 | CV2839886 | single nucleotide variant | NM_001136219.3(FCGR2A):c.943A>G (p.Ser315Gly) | not provided [RCV003456673] | uncertain significance | 1 | 161518137 | 161518137 | Human | | name |
| 8599968 | CV29862 | single nucleotide variant | NM_001136219.3(FCGR2A):c.500A>G (p.His167Arg) | Lupus nephritis, susceptibility to [RCV000015946]|Malaria, severe, susceptibility to [RCV000054529]|Pseudomonas aeruginosa, susceptibility to chronic infection by, in cystic fibrosis [RCV000015947]|not provided [RCV004713172]|not specified [RCV000454909] | risk factor|benign|drug response | 1 | 161509955 | 161509955 | Human | 19 | name |
| 405725636 | CV3256796 | single nucleotide variant | NM_001136219.3(FCGR2A):c.308C>T (p.Thr103Met) | not specified [RCV004389341] | uncertain significance | 1 | 161506535 | 161506535 | Human | | name |
| 405725647 | CV3256797 | single nucleotide variant | NM_001136219.3(FCGR2A):c.341C>T (p.Pro114Leu) | not specified [RCV004389342] | uncertain significance | 1 | 161506568 | 161506568 | Human | | name |
| 405741554 | CV3256799 | single nucleotide variant | NM_001136219.3(FCGR2A):c.799A>C (p.Ile267Leu) | not specified [RCV004391415] | uncertain significance | 1 | 161517993 | 161517993 | Human | | name |
| 405741561 | CV3256800 | single nucleotide variant | NM_001136219.3(FCGR2A):c.943A>T (p.Ser315Cys) | not specified [RCV004391416] | uncertain significance | 1 | 161518137 | 161518137 | Human | | name |
| 405741570 | CV3256801 | single nucleotide variant | NM_001136219.3(FCGR2A):c.944G>A (p.Ser315Asn) | not specified [RCV004391417] | uncertain significance | 1 | 161518138 | 161518138 | Human | | name |
| 407482861 | CV3438823 | single nucleotide variant | NM_001136219.3(FCGR2A):c.865A>G (p.Met289Val) | not specified [RCV004618467] | uncertain significance | 1 | 161518059 | 161518059 | Human | | name |
| 407482867 | CV3438824 | single nucleotide variant | NM_001136219.3(FCGR2A):c.689C>T (p.Ala230Val) | not specified [RCV004618468] | uncertain significance | 1 | 161510903 | 161510903 | Human | | name |
| 597739356 | CV3675947 | single nucleotide variant | NM_001136219.3(FCGR2A):c.790C>T (p.Arg264Cys) | not specified [RCV004921243] | uncertain significance | 1 | 161517984 | 161517984 | Human | | name |
| 597739361 | CV3675948 | single nucleotide variant | NM_001136219.3(FCGR2A):c.756T>A (p.Asp252Glu) | not specified [RCV004921244] | uncertain significance | 1 | 161513908 | 161513908 | Human | | name |
| 597739366 | CV3675949 | single nucleotide variant | NM_001136219.3(FCGR2A):c.512C>A (p.Thr171Asn) | not specified [RCV004921245] | likely benign | 1 | 161509967 | 161509967 | Human | | name |
| 597739371 | CV3675950 | single nucleotide variant | NM_001136219.3(FCGR2A):c.509C>T (p.Pro170Leu) | not specified [RCV004921246] | uncertain significance | 1 | 161509964 | 161509964 | Human | | name |
| 597739375 | CV3675951 | single nucleotide variant | NM_001136219.3(FCGR2A):c.758C>T (p.Pro253Leu) | not specified [RCV004921247] | uncertain significance | 1 | 161513910 | 161513910 | Human | | name |
| 597739380 | CV3675952 | single nucleotide variant | NM_001136219.3(FCGR2A):c.859G>A (p.Gly287Ser) | not specified [RCV004921248] | uncertain significance | 1 | 161518053 | 161518053 | Human | | name |
| 597739385 | CV3675953 | single nucleotide variant | NM_001136219.3(FCGR2A):c.305A>G (p.Tyr102Cys) | not specified [RCV004921249] | uncertain significance | 1 | 161506532 | 161506532 | Human | | name |
| 597739394 | CV3675955 | single nucleotide variant | NM_001136219.3(FCGR2A):c.934C>A (p.His312Asn) | not specified [RCV004921251] | uncertain significance | 1 | 161518128 | 161518128 | Human | | name |
| 597739399 | CV3675956 | single nucleotide variant | NM_001136219.3(FCGR2A):c.901A>G (p.Lys301Glu) | not specified [RCV004921252] | uncertain significance | 1 | 161518095 | 161518095 | Human | | name |
| 597854401 | CV3762371 | single nucleotide variant | NM_001136219.3(FCGR2A):c.386C>T (p.Pro129Leu) | not specified [RCV005088287] | uncertain significance | 1 | 161509841 | 161509841 | Human | | name |
| 598124348 | CV3885171 | single nucleotide variant | NM_001136219.3(FCGR2A):c.851C>T (p.Ala284Val) | not specified [RCV005239748] | uncertain significance | 1 | 161518045 | 161518045 | Human | | name |
| 598229279 | CV3959078 | single nucleotide variant | NM_001136219.3(FCGR2A):c.581C>T (p.Thr194Met) | not specified [RCV005342047] | uncertain significance | 1 | 161510036 | 161510036 | Human | | name |
| 598271871 | CV3959080 | single nucleotide variant | NM_001136219.3(FCGR2A):c.906C>A (p.Asn302Lys) | not specified [RCV005327839] | uncertain significance | 1 | 161518100 | 161518100 | Human | | name |
| 617152975 | CV4020849 | single nucleotide variant | NM_001136219.3(FCGR2A):c.839A>C (p.Asp280Ala) | not provided [RCV005428602] | likely benign | 1 | 161518033 | 161518033 | Human | | name |
| 15200317 | CV718333 | single nucleotide variant | NM_001136219.3(FCGR2A):c.733C>T (p.Arg245Trp) | not provided [RCV000890879] | benign | 1 | 161510947 | 161510947 | Human | | name |
