FAM162A
family with sequence similarity 162 member A
Summary
Involved in cellular response to hypoxia; positive regulation of apoptotic process; and positive regulation of release of cytochrome c from mitochondria. Located in cytosol and mitochondrion. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants17 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2472498243 | 3:122,103,123 | T/G | — | uncertain significance |
| rs568788103 | 3:122,110,268 | T/C | — | — |
| rs7635930 | 3:122,112,557 | G/C | intron variant | — |
| rs9834975 | 3:122,117,663 | A/G | — | — |
| rs73188388 | 3:122,118,076 | C/T | intron variant | — |
| rs745565586 | 3:122,121,717 | G/A | — | likely benign |
| rs147029695 | 3:122,122,215 | G/A | regulatory region variant | — |
| rs199848888 | 3:122,123,179 | A/G | — | uncertain significance |
| rs12107092 | 3:122,123,848 | C/T | intron variant | — |
| rs372529727 | 3:122,126,152 | G/C | — | uncertain significance |
| rs1192359264 | 3:122,126,163 | G/A | — | uncertain significance |
| rs2472521235 | 3:122,126,180 | C/G | — | likely benign |
| rs2472521276 | 3:122,126,223 | T/C | — | uncertain significance |
| rs181265174 | 3:122,128,589 | G/A | — | uncertain significance |
| rs1341257535 | 3:122,128,635 | C/T | — | uncertain significance |
| rs73188392 | 3:122,128,638 | G/A | — | uncertain significance |
| rs748176562 | 3:122,128,668 | A/G | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.