FAM117A
family with sequence similarity 117 member A
Known Variants29 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2544044859 | 17:47,788,624 | A/G | — | uncertain significance |
| rs375320243 | 17:47,788,723 | C/T | — | uncertain significance |
| rs144428416 | 17:47,788,784 | G/A | missense variant | — |
| rs753106696 | 17:47,794,908 | C/T | — | uncertain significance |
| rs758052826 | 17:47,794,917 | G/A | — | uncertain significance |
| rs2544053613 | 17:47,794,926 | C/T | — | uncertain significance |
| rs2544053841 | 17:47,795,003 | A/C | — | uncertain significance |
| rs774498092 | 17:47,795,004 | G/A | — | uncertain significance |
| rs140500484 | 17:47,795,052 | G/A | — | uncertain significance |
| rs368889183 | 17:47,797,216 | C/T | — | uncertain significance |
| rs780032318 | 17:47,797,246 | G/C | — | uncertain significance |
| rs2544058731 | 17:47,797,711 | G/A | — | uncertain significance |
| rs774907028 | 17:47,797,712 | G/T | — | uncertain significance |
| rs751602289 | 17:47,797,753 | T/C | — | likely benign |
| rs755049183 | 17:47,797,755 | C/T | — | uncertain significance |
| rs781423934 | 17:47,797,756 | G/A | — | uncertain significance |
| rs143324421 | 17:47,799,899 | G/A | — | uncertain significance |
| rs2544072871 | 17:47,809,936 | A/G | — | uncertain significance |
| rs2544072986 | 17:47,809,989 | C/T | — | uncertain significance |
| rs373170061 | 17:47,810,077 | C/T | — | uncertain significance |
| rs769818449 | 17:47,811,894 | C/T | — | — |
| rs77522818 | 17:47,817,373 | A/T | regulatory region variant | — |
| rs1435631311 | 17:47,841,281 | G/T | — | uncertain significance |
| rs2073734170 | 17:47,841,338 | G/A | — | uncertain significance |
| rs773300848 | 17:47,841,403 | G/T | — | uncertain significance |
| rs759887702 | 17:47,841,427 | C/T | — | uncertain significance |
| rs2544100681 | 17:47,841,440 | C/T | — | uncertain significance |
| rs12949906 | 17:47,847,079 | A/G | intron variant | — |
| rs575705078 | 17:47,856,909 | A/G | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.