FAM181A
family with sequence similarity 181 member A
Summary
Located in cytoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants27 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs11160152 | 14:94,387,803 | C/A | — | — |
| rs778270343 | 14:94,391,700 | C/T | — | uncertain significance |
| rs117161928 | 14:94,391,705 | A/T | missense variant | — |
| rs748244971 | 14:94,394,575 | G/A | — | likely benign |
| rs147412568 | 14:94,394,629 | G/C | — | uncertain significance |
| rs752834933 | 14:94,394,728 | C/T | — | uncertain significance |
| rs769266540 | 14:94,394,729 | G/A | — | uncertain significance |
| rs779986039 | 14:94,394,734 | G/A | — | uncertain significance |
| rs144265486 | 14:94,394,744 | G/A | — | uncertain significance |
| rs777310102 | 14:94,394,780 | A/G | — | uncertain significance |
| rs372111603 | 14:94,394,791 | C/T | — | uncertain significance |
| rs1300866846 | 14:94,394,827 | C/T | — | uncertain significance |
| rs145475417 | 14:94,394,911 | G/A | — | uncertain significance |
| rs371991985 | 14:94,394,916 | C/G | — | uncertain significance |
| rs752651380 | 14:94,394,939 | C/T | — | uncertain significance |
| rs571368703 | 14:94,395,094 | G/C | — | uncertain significance |
| rs200507444 | 14:94,395,137 | A/C | — | uncertain significance |
| rs766014903 | 14:94,395,214 | G/C | — | uncertain significance |
| rs149056402 | 14:94,395,218 | C/T | — | uncertain significance |
| rs2503466779 | 14:94,395,232 | G/A | — | uncertain significance |
| rs138636477 | 14:94,395,244 | G/C | — | uncertain significance |
| rs199608834 | 14:94,395,250 | C/T | — | uncertain significance |
| rs371287987 | 14:94,395,251 | G/A | — | uncertain significance |
| rs776549246 | 14:94,395,266 | G/A | — | uncertain significance |
| rs556211566 | 14:94,395,341 | C/A | — | uncertain significance |
| rs147001146 | 14:94,395,407 | T/C | — | likely benign |
| rs145841226 | 14:94,395,833 | C/T | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.