FAM222A
family with sequence similarity 222 member A
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs77346308 | 12:110,153,675 | C/T | intron variant | — |
| rs7310085 | 12:110,164,377 | G/A | regulatory region variant | — |
| rs545512808 | 12:110,181,994 | C/T | — | uncertain significance |
| rs369986211 | 12:110,182,004 | G/A | — | uncertain significance |
| rs146405681 | 12:110,182,007 | C/G | — | uncertain significance |
| rs1889106772 | 12:110,205,817 | G/A | — | uncertain significance |
| rs1255332926 | 12:110,205,822 | G/T | — | uncertain significance |
| rs567100977 | 12:110,205,837 | A/G | — | uncertain significance |
| rs201342971 | 12:110,205,880 | A/T | — | uncertain significance |
| rs771798501 | 12:110,205,936 | C/T | — | uncertain significance |
| rs146163512 | 12:110,205,963 | C/T | — | uncertain significance |
| rs140190262 | 12:110,205,996 | C/A | — | uncertain significance |
| rs2548699145 | 12:110,206,017 | C/T | — | uncertain significance |
| rs763757845 | 12:110,206,018 | A/T | missense variant | pathogenic |
| rs1889115876 | 12:110,206,019 | C/G | — | uncertain significance |
| rs774565291 | 12:110,206,063 | T/C | — | uncertain significance |
| rs533079318 | 12:110,206,134 | A/G | — | uncertain significance |
| rs764817979 | 12:110,206,155 | G/A | — | uncertain significance |
| rs543160077 | 12:110,206,172 | G/A | — | benign |
| rs201397662 | 12:110,206,281 | C/T | — | uncertain significance |
| rs201283705 | 12:110,206,294 | G/A | — | uncertain significance |
| rs1889131723 | 12:110,206,312 | C/A | — | uncertain significance |
| rs775233169 | 12:110,206,356 | C/G | — | uncertain significance |
| rs370934435 | 12:110,206,380 | G/A | — | uncertain significance |
| rs778158113 | 12:110,206,423 | C/T | — | uncertain significance |
| rs199593023 | 12:110,206,494 | C/T | — | uncertain significance |
| rs754400731 | 12:110,206,578 | G/A | — | uncertain significance |
| rs369923455 | 12:110,206,588 | A/G | — | uncertain significance |
| rs542798024 | 12:110,206,610 | G/A | — | benign |
| rs201569829 | 12:110,206,630 | C/T | — | uncertain significance |
| rs200880090 | 12:110,206,636 | G/A | — | uncertain significance |
| rs754643198 | 12:110,206,690 | G/A | — | uncertain significance |
| rs372613814 | 12:110,206,772 | G/A | — | likely benign |
| rs745617925 | 12:110,206,777 | C/T | — | uncertain significance |
| rs373168309 | 12:110,206,812 | T/A | — | uncertain significance |
| rs377710576 | 12:110,206,825 | C/T | — | uncertain significance |
| rs560155848 | 12:110,206,843 | C/T | — | uncertain significance |
| rs777927919 | 12:110,206,855 | C/T | — | uncertain significance |
| rs746362704 | 12:110,206,867 | G/A | — | uncertain significance |
| rs111838477 | 12:110,206,871 | G/A | — | likely benign |
| rs561023021 | 12:110,206,900 | C/T | — | uncertain significance |
| rs756389699 | 12:110,206,917 | A/T | — | uncertain significance |
| rs201840129 | 12:110,207,044 | G/A | — | uncertain significance |
| rs142286258 | 12:110,207,046 | C/T | — | likely benign |
| rs1889170885 | 12:110,207,057 | C/G | — | uncertain significance |
| rs537650643 | 12:110,207,073 | C/G | — | uncertain significance |
| rs150508057 | 12:110,207,078 | A/G | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.