FAM107B
family with sequence similarity 107 member B
Summary
Predicted to act upstream of or within sensory perception of sound. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants20 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs373444074 | 10:14,563,271 | T/C | — | uncertain significance |
| rs34265970 | 10:14,563,299 | G/C | — | benign |
| rs1845684918 | 10:14,563,924 | T/G | — | uncertain significance |
| rs776506034 | 10:14,564,000 | G/T | — | uncertain significance |
| rs1564528553 | 10:14,572,376 | C/T | — | uncertain significance |
| rs773674410 | 10:14,572,377 | G/A | — | uncertain significance |
| rs367679632 | 10:14,572,400 | A/G | — | uncertain significance |
| rs772869644 | 10:14,572,490 | T/C | — | uncertain significance |
| rs1472637711 | 10:14,572,491 | G/C | — | uncertain significance |
| rs2491619656 | 10:14,572,506 | G/A | — | uncertain significance |
| rs7068157 | 10:14,615,644 | G/A | regulatory region variant | — |
| rs4750535 | 10:14,633,024 | C/T | intron variant | — |
| rs717068 | 10:14,653,045 | T/A | — | — |
| rs114622288 | 10:14,663,844 | G/T | — | — |
| rs61842737 | 10:14,680,617 | C/T | — | — |
| rs35772238 | 10:14,686,781 | A/G | intron variant | — |
| rs3847358 | 10:14,686,953 | C/G | — | — |
| rs149371316 | 10:14,709,658 | G/A | — | benign |
| rs151236833 | 10:14,816,259 | G/A | — | likely benign |
| rs141291914 | 10:14,816,315 | C/T | — | benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.