FAM227A
family with sequence similarity 227 member A
Known Variants47 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1013338 | 22:38,974,154 | C/A | downstream gene variant | — |
| rs1013339 | 22:38,974,680 | C/T | downstream gene variant | — |
| rs186341152 | 22:38,978,909 | G/A | missense variant | — |
| rs2518309288 | 22:38,982,155 | A/C | — | uncertain significance |
| rs2090802363 | 22:38,982,158 | T/C | — | uncertain significance |
| rs761584517 | 22:38,982,186 | C/T | — | uncertain significance |
| rs936296330 | 22:38,982,195 | C/T | — | uncertain significance |
| rs527799253 | 22:38,987,517 | C/T | — | uncertain significance |
| rs79198494 | 22:38,987,519 | G/A | — | uncertain significance |
| rs78539182 | 22:38,987,526 | G/T | — | uncertain significance |
| rs1364930930 | 22:38,987,534 | T/C | — | uncertain significance |
| rs5757161 | 22:38,990,662 | G/T | — | — |
| rs998405543 | 22:38,993,248 | A/G | — | uncertain significance |
| rs772959416 | 22:38,993,256 | C/G | — | uncertain significance |
| rs751226372 | 22:38,993,287 | T/C | — | uncertain significance |
| rs565247823 | 22:38,993,303 | G/A | — | uncertain significance |
| rs1366889642 | 22:38,993,308 | T/G | — | uncertain significance |
| rs1206080169 | 22:38,993,344 | T/C | — | uncertain significance |
| rs5757162 | 22:38,993,370 | C/T | intron variant | — |
| rs780436534 | 22:38,995,854 | C/G | — | uncertain significance |
| rs2518462303 | 22:39,003,477 | G/C | — | uncertain significance |
| rs1350488237 | 22:39,003,480 | G/A | — | likely benign |
| rs5750644 | 22:39,009,135 | A/T | intron variant | — |
| rs1028758884 | 22:39,016,249 | G/T | — | uncertain significance |
| rs559284041 | 22:39,019,219 | G/A | — | uncertain significance |
| rs201824717 | 22:39,019,225 | G/C | — | uncertain significance |
| rs138823795 | 22:39,019,254 | C/A | — | uncertain significance |
| rs1314076033 | 22:39,019,278 | T/C | — | uncertain significance |
| rs969551506 | 22:39,022,203 | T/C | — | uncertain significance |
| rs376632432 | 22:39,022,230 | C/T | — | uncertain significance |
| rs1361663502 | 22:39,024,286 | A/C | — | uncertain significance |
| rs777640180 | 22:39,024,341 | T/C | — | uncertain significance |
| rs2518634881 | 22:39,024,892 | G/C | — | uncertain significance |
| rs1220435130 | 22:39,024,895 | A/G | — | uncertain significance |
| rs9306328 | 22:39,028,913 | C/T | intron variant | — |
| rs780309203 | 22:39,032,501 | C/T | — | uncertain significance |
| rs370979052 | 22:39,032,526 | G/A | — | uncertain significance |
| rs776588220 | 22:39,034,756 | T/C | — | uncertain significance |
| rs1682173008 | 22:39,035,666 | C/T | — | uncertain significance |
| rs4821802 | 22:39,037,552 | A/G | intron variant | — |
| rs9607557 | 22:39,040,279 | G/A | regulatory region variant | — |
| rs7289855 | 22:39,042,221 | G/T | intron variant | — |
| rs577824828 | 22:39,046,083 | G/A | — | uncertain significance |
| rs769478191 | 22:39,046,086 | C/T | — | uncertain significance |
| rs1204864339 | 22:39,046,115 | A/G | — | uncertain significance |
| rs933043753 | 22:39,046,119 | G/A | — | uncertain significance |
| rs942934493 | 22:39,050,133 | G/C | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.