FAM234A
family with sequence similarity 234 member A
Summary
Located in cell surface. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants72 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs529547050 | 16:283,841 | T/A | — | — |
| rs112832450 | 16:284,986 | C/T | regulatory region variant | — |
| rs533614130 | 16:286,000 | A/G | — | — |
| rs191852210 | 16:286,242 | A/G | downstream gene variant | — |
| rs186692714 | 16:288,044 | T/G | intron variant | — |
| rs182103652 | 16:288,348 | C/T | intron variant | — |
| rs187651195 | 16:288,541 | A/C | — | — |
| rs9788833 | 16:292,772 | T/A | — | — |
| rs55985014 | 16:294,189 | G/C | intron variant | — |
| rs112316985 | 16:295,957 | G/A | upstream gene variant | — |
| rs143263021 | 16:296,567 | C/T | upstream gene variant | — |
| rs13339636 | 16:298,588 | A/G | upstream gene variant | — |
| rs13331259 | 16:299,923 | A/G | intron variant | — |
| rs151330263 | 16:302,161 | A/G | intron variant | — |
| rs142476478 | 16:302,626 | C/T | — | — |
| rs8047053 | 16:303,663 | T/C | intron variant | — |
| rs1157022145 | 16:304,446 | C/T | — | uncertain significance |
| rs773073386 | 16:304,483 | A/G | — | uncertain significance |
| rs2548383793 | 16:304,521 | A/T | — | uncertain significance |
| rs1395066752 | 16:304,535 | G/T | — | uncertain significance |
| rs192602168 | 16:304,549 | G/A | — | uncertain significance |
| rs765566976 | 16:304,564 | C/A | — | uncertain significance |
| rs1278306820 | 16:304,570 | T/C | — | uncertain significance |
| rs756526364 | 16:304,602 | T/G | — | uncertain significance |
| rs7189020 | 16:304,803 | A/C | — | — |
| rs8045544 | 16:308,002 | G/C | — | — |
| rs1122794 | 16:309,155 | C/A | intron variant | — |
| rs552685505 | 16:309,492 | C/G | — | uncertain significance |
| rs907651253 | 16:309,496 | C/T | — | likely benign |
| rs13335497 | 16:310,005 | G/A | — | benign |
| rs201735340 | 16:310,018 | A/T | — | uncertain significance |
| rs770280178 | 16:310,022 | C/T | — | uncertain significance |
| rs372933829 | 16:310,137 | C/G | — | uncertain significance |
| rs13335629 | 16:310,380 | G/A | intron variant | — |
| rs375399489 | 16:311,466 | G/A | — | likely benign |
| rs200842636 | 16:311,479 | C/G | — | uncertain significance |
| rs1596841053 | 16:311,498 | C/T | — | likely benign |
| rs73486203 | 16:311,506 | G/A | — | benign |
| rs2239741 | 16:312,015 | T/C | intron variant | — |
| rs376175413 | 16:312,170 | G/C | — | uncertain significance |
| rs370881261 | 16:312,218 | C/G | — | uncertain significance |
| rs759550507 | 16:312,461 | G/A | — | uncertain significance |
| rs199764048 | 16:313,261 | C/T | — | likely benign |
| rs778805979 | 16:313,289 | G/A | — | uncertain significance |
| rs371412736 | 16:313,322 | G/T | — | uncertain significance |
| rs567807471 | 16:313,335 | C/G | — | likely benign |
| rs1243627339 | 16:313,352 | G/A | — | uncertain significance |
| rs375467779 | 16:313,365 | C/T | — | uncertain significance |
| rs200772333 | 16:313,701 | A/C | — | uncertain significance |
| rs750278669 | 16:313,706 | A/G | — | likely benign |
| rs575006186 | 16:313,715 | C/T | — | uncertain significance |
| rs2548426915 | 16:313,725 | C/A | — | uncertain significance |
| rs772106861 | 16:313,766 | G/A | — | likely benign |
| rs375509833 | 16:314,045 | G/A | — | likely benign |
| rs768717459 | 16:314,061 | C/T | — | uncertain significance |
| rs373393536 | 16:314,107 | C/T | — | likely benign |
| rs149439168 | 16:314,143 | C/G | — | benign |
| rs751322019 | 16:314,169 | C/T | — | likely benign |
| rs374928451 | 16:314,619 | G/C | — | likely benign |
| rs754703794 | 16:314,628 | C/T | — | uncertain significance |
| rs144208371 | 16:314,662 | C/T | — | uncertain significance |
| rs754935510 | 16:314,665 | G/T | — | uncertain significance |
| rs9924561 | 16:314,780 | G/A | downstream gene variant | — |
| rs533890166 | 16:314,839 | G/A | — | uncertain significance |
| rs201652010 | 16:314,845 | A/G | — | likely benign |
| rs1309873371 | 16:314,920 | G/T | — | uncertain significance |
| rs577904477 | 16:314,944 | C/G | — | uncertain significance |
| rs1008005525 | 16:314,995 | C/T | — | uncertain significance |
| rs140871153 | 16:315,008 | A/G | — | benign |
| rs739997 | 16:316,860 | T/C | downstream gene variant | — |
| rs77817084 | 16:316,945 | G/A | downstream gene variant | — |
| rs57268939 | 16:319,547 | T/C | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.