FAM171A1
family with sequence similarity 171 member A1
Summary
Involved in regulation of cell shape and stress fiber assembly. Located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants56 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1384845378 | 10:15,254,996 | T/A | — | uncertain significance |
| rs769373116 | 10:15,255,015 | C/T | — | uncertain significance |
| rs748814910 | 10:15,255,018 | G/A | — | uncertain significance |
| rs1190547313 | 10:15,255,095 | A/C | — | uncertain significance |
| rs775593175 | 10:15,255,156 | T/C | — | uncertain significance |
| rs1564611142 | 10:15,255,167 | G/A | — | uncertain significance |
| rs751731015 | 10:15,255,170 | C/T | — | uncertain significance |
| rs1350057360 | 10:15,255,174 | C/A | — | likely benign |
| rs779708676 | 10:15,255,183 | C/T | — | uncertain significance |
| rs200146894 | 10:15,255,204 | C/T | — | uncertain significance |
| rs1833917435 | 10:15,255,273 | G/T | — | uncertain significance |
| rs2491453170 | 10:15,255,288 | G/A | — | uncertain significance |
| rs2491453352 | 10:15,255,341 | G/A | — | uncertain significance |
| rs772071145 | 10:15,255,414 | T/C | — | uncertain significance |
| rs773380801 | 10:15,255,422 | T/C | — | uncertain significance |
| rs1833920632 | 10:15,255,449 | T/C | — | uncertain significance |
| rs757886041 | 10:15,255,479 | G/A | — | uncertain significance |
| rs146450035 | 10:15,255,497 | C/G | — | uncertain significance |
| rs772385137 | 10:15,255,498 | C/G | — | uncertain significance |
| rs141302989 | 10:15,255,658 | G/C | — | uncertain significance |
| rs150380126 | 10:15,255,683 | G/A | — | uncertain significance |
| rs1298779791 | 10:15,255,690 | T/A | — | uncertain significance |
| rs761364473 | 10:15,255,693 | G/T | — | uncertain significance |
| rs199915147 | 10:15,255,720 | C/A | — | uncertain significance |
| rs763189702 | 10:15,255,800 | T/C | — | uncertain significance |
| rs1206270248 | 10:15,255,813 | C/T | — | uncertain significance |
| rs372962927 | 10:15,255,870 | C/T | — | uncertain significance |
| rs1833930298 | 10:15,255,938 | C/G | — | uncertain significance |
| rs148721770 | 10:15,256,035 | G/A | — | uncertain significance |
| rs2491456714 | 10:15,256,139 | T/C | — | uncertain significance |
| rs377674623 | 10:15,256,142 | T/C | — | uncertain significance |
| rs145662406 | 10:15,256,169 | T/C | — | uncertain significance |
| rs1320801883 | 10:15,256,175 | G/C | — | uncertain significance |
| rs148829329 | 10:15,256,233 | T/C | — | uncertain significance |
| rs746303349 | 10:15,256,265 | T/C | — | uncertain significance |
| rs781122848 | 10:15,256,553 | G/A | — | uncertain significance |
| rs76394384 | 10:15,256,563 | G/C | — | uncertain significance |
| rs144702270 | 10:15,258,001 | T/C | — | uncertain significance |
| rs2491472292 | 10:15,262,959 | C/A | — | uncertain significance |
| rs549652490 | 10:15,271,587 | T/C | — | — |
| rs111276643 | 10:15,281,686 | G/A | intron variant | — |
| rs767112266 | 10:15,290,664 | G/A | — | uncertain significance |
| rs201873537 | 10:15,290,770 | C/T | — | uncertain significance |
| rs184600985 | 10:15,290,776 | C/T | — | uncertain significance |
| rs778885958 | 10:15,290,805 | G/T | — | uncertain significance |
| rs532778999 | 10:15,296,743 | C/T | — | uncertain significance |
| rs780972854 | 10:15,296,797 | G/A | — | uncertain significance |
| rs1192523077 | 10:15,296,798 | C/T | — | uncertain significance |
| rs748772452 | 10:15,296,810 | T/C | — | uncertain significance |
| rs746749391 | 10:15,296,858 | C/T | — | uncertain significance |
| rs747672439 | 10:15,296,873 | G/C | — | uncertain significance |
| rs1481327510 | 10:15,317,869 | C/A | — | uncertain significance |
| rs753456824 | 10:15,325,885 | C/T | — | uncertain significance |
| rs375338905 | 10:15,326,036 | T/A | — | uncertain significance |
| rs143775633 | 10:15,326,090 | C/T | — | uncertain significance |
| rs2491677473 | 10:15,412,994 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.