FAM118A

family with sequence similarity 118 member A

Summary

Enables identical protein binding activity. Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]

Known Variants25 total

rsidPosition (GRCh37)AllelesClassClinVar
rs1216755522:45,705,399T/Gregulatory region variant—
rs20170113422:45,719,060T/G—uncertain significance
rs76223189722:45,719,078C/T—uncertain significance
rs14968006022:45,719,141G/A—uncertain significance
rs20183043722:45,719,176C/T—likely benign
rs14444707522:45,719,183G/A—uncertain significance
rs14392469522:45,719,222G/A—uncertain significance
rs74965102522:45,719,234G/A—uncertain significance
rs77705881322:45,719,261C/T—uncertain significance
rs73817022:45,721,196C/Tintron variant—
rs73817122:45,721,284T/G——
rs14068339422:45,723,798C/T—uncertain significance
rs208540525422:45,723,804C/G—uncertain significance
rs75193024222:45,723,864A/C—uncertain significance
rs14701863622:45,723,883A/T—uncertain significance
rs251820193322:45,723,936A/G—uncertain significance
rs600759222:45,724,727G/C——
rs235062822:45,725,276G/C——
rs73670222:45,725,600A/C——
rs37227651922:45,726,577G/A—uncertain significance
rs37440172422:45,728,498G/A—uncertain significance
rs20062280622:45,728,540C/G—uncertain significance
rs119884230122:45,732,229G/T—uncertain significance
rs37530492722:45,732,262G/A—uncertain significance
rs77337928122:45,732,263T/G—uncertain significance

Gene information from NCBI Gene. Variant classifications from ClinVar.