FAM185A
family with sequence similarity 185 member A
Summary
Located in mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants26 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs375256358 | 7:102,388,400 | C/G | — | — |
| rs765407128 | 7:102,389,786 | C/G | — | uncertain significance |
| rs2535204424 | 7:102,389,853 | T/G | — | uncertain significance |
| rs897158003 | 7:102,389,995 | G/A | — | uncertain significance |
| rs1248931505 | 7:102,392,139 | G/T | — | uncertain significance |
| rs1389036238 | 7:102,392,181 | A/G | — | uncertain significance |
| rs773379551 | 7:102,392,208 | T/C | — | uncertain significance |
| rs973812582 | 7:102,392,246 | A/G | — | uncertain significance |
| rs748485905 | 7:102,401,730 | T/C | — | uncertain significance |
| rs770103710 | 7:102,401,766 | C/A | — | uncertain significance |
| rs1418698030 | 7:102,401,834 | G/C | — | uncertain significance |
| rs1426593458 | 7:102,401,837 | A/T | — | uncertain significance |
| rs80121318 | 7:102,410,096 | A/G | intron variant | — |
| rs139722172 | 7:102,410,477 | C/G | intron variant | — |
| rs761520461 | 7:102,412,880 | T/C | — | uncertain significance |
| rs768437331 | 7:102,417,700 | A/G | — | uncertain significance |
| rs1795126963 | 7:102,417,711 | G/A | — | uncertain significance |
| rs1047217888 | 7:102,417,733 | A/C | — | uncertain significance |
| rs575177914 | 7:102,417,745 | T/C | — | uncertain significance |
| rs1326935498 | 7:102,427,847 | G/T | — | uncertain significance |
| rs375146574 | 7:102,427,890 | G/A | — | likely benign |
| rs3972456 | 7:102,436,907 | G/A | — | — |
| rs6949391 | 7:102,446,863 | C/A | — | — |
| rs145625209 | 7:102,448,760 | C/T | — | uncertain significance |
| rs76779367 | 7:102,451,590 | A/G | regulatory region variant | — |
| rs76165167 | 7:102,479,719 | C/T | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.