FAM117B
family with sequence similarity 117 member B
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs775984471 | 2:203,499,929 | C/T | — | uncertain significance |
| rs2468727642 | 2:203,499,944 | A/G | — | uncertain significance |
| rs1689658532 | 2:203,499,965 | G/A | — | uncertain significance |
| rs1689660738 | 2:203,500,046 | C/G | — | uncertain significance |
| rs1312608410 | 2:203,500,088 | G/A | — | uncertain significance |
| rs1402528554 | 2:203,500,160 | G/A | — | uncertain significance |
| rs1284581659 | 2:203,500,167 | G/A | — | uncertain significance |
| rs1689666401 | 2:203,500,208 | A/G | — | uncertain significance |
| rs758079604 | 2:203,500,248 | C/A | — | uncertain significance |
| rs1689668102 | 2:203,500,269 | C/T | — | uncertain significance |
| rs2468728459 | 2:203,500,283 | C/T | — | uncertain significance |
| rs979329522 | 2:203,500,368 | C/A | — | uncertain significance |
| rs1385382422 | 2:203,500,449 | C/T | — | uncertain significance |
| rs1689673524 | 2:203,500,452 | C/T | — | uncertain significance |
| rs1488386346 | 2:203,500,462 | C/G | — | uncertain significance |
| rs918901738 | 2:203,500,472 | C/T | — | uncertain significance |
| rs72926986 | 2:203,519,264 | G/T | intron variant | — |
| rs72926990 | 2:203,520,420 | G/A | intron variant | — |
| rs55866932 | 2:203,523,042 | A/G | intron variant | — |
| rs11694172 | 2:203,532,304 | A/G | intron variant | — |
| rs113138131 | 2:203,545,127 | A/G | — | — |
| rs1690703105 | 2:203,560,637 | C/G | — | uncertain significance |
| rs780227097 | 2:203,560,652 | G/A | — | uncertain significance |
| rs772577240 | 2:203,560,679 | C/T | — | uncertain significance |
| rs72928934 | 2:203,562,740 | A/T | — | — |
| rs6721748 | 2:203,578,306 | C/G | intron variant | — |
| rs191390916 | 2:203,579,866 | C/G | — | — |
| rs1691215492 | 2:203,589,643 | G/A | — | uncertain significance |
| rs368920313 | 2:203,589,694 | C/T | — | uncertain significance |
| rs773045277 | 2:203,589,695 | G/A | — | uncertain significance |
| rs945876506 | 2:203,589,718 | G/A | — | uncertain significance |
| rs564095694 | 2:203,620,264 | C/T | — | uncertain significance |
| rs2468860486 | 2:203,620,297 | C/G | — | uncertain significance |
| rs750404246 | 2:203,620,400 | T/G | — | uncertain significance |
| rs552505798 | 2:203,622,077 | A/G | — | uncertain significance |
| rs149565894 | 2:203,622,099 | A/G | — | uncertain significance |
| rs186257616 | 2:203,622,126 | C/T | — | uncertain significance |
| rs1001873887 | 2:203,623,965 | A/G | — | uncertain significance |
| rs770995798 | 2:203,630,347 | A/T | — | uncertain significance |
| rs776110893 | 2:203,630,371 | G/A | — | likely benign |
| rs752621082 | 2:203,630,414 | G/T | — | uncertain significance |
| rs746725640 | 2:203,630,433 | G/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.