FAM168A
family with sequence similarity 168 member A
Summary
Involved in positive regulation of base-excision repair. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants14 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs371613362 | 11:73,118,616 | T/C | — | uncertain significance |
| rs367570839 | 11:73,118,658 | G/A | — | uncertain significance |
| rs769799497 | 11:73,118,661 | G/A | — | uncertain significance |
| rs749363209 | 11:73,120,574 | C/T | — | uncertain significance |
| rs774913792 | 11:73,120,580 | C/T | — | uncertain significance |
| rs12290623 | 11:73,121,872 | C/G | downstream gene variant | — |
| rs7952686 | 11:73,128,503 | C/T | intron variant | — |
| rs368582493 | 11:73,141,776 | T/C | — | uncertain significance |
| rs78975595 | 11:73,146,791 | T/C | intron variant | — |
| rs562758668 | 11:73,179,498 | C/T | — | uncertain significance |
| rs113988287 | 11:73,195,669 | A/C | intron variant | — |
| rs147351254 | 11:73,197,626 | C/G | intron variant | — |
| rs1145656 | 11:73,305,859 | C/A | intron variant | — |
| rs7943721 | 11:73,309,393 | G/A | regulatory region variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.