FAM163B
family with sequence similarity 163 member B
Summary
Predicted to be located in membrane. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants34 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs745401450 | 9:136,444,190 | A/C | — | uncertain significance |
| rs760760094 | 9:136,444,218 | C/T | — | uncertain significance |
| rs755651229 | 9:136,444,241 | G/A | — | uncertain significance |
| rs749785225 | 9:136,444,254 | C/T | — | uncertain significance |
| rs567087803 | 9:136,444,258 | C/G | — | uncertain significance |
| rs772227656 | 9:136,444,270 | G/T | — | uncertain significance |
| rs1337469730 | 9:136,444,277 | T/C | — | uncertain significance |
| rs377564199 | 9:136,444,301 | A/G | — | uncertain significance |
| rs755778016 | 9:136,444,304 | A/G | — | uncertain significance |
| rs779409568 | 9:136,444,322 | G/A | — | uncertain significance |
| rs970052148 | 9:136,444,326 | G/A | — | uncertain significance |
| rs1321039462 | 9:136,444,354 | G/C | — | uncertain significance |
| rs2538250029 | 9:136,444,368 | T/A | — | uncertain significance |
| rs765973375 | 9:136,444,385 | G/A | — | uncertain significance |
| rs61742003 | 9:136,444,421 | G/A | — | uncertain significance |
| rs1291969735 | 9:136,444,433 | G/A | — | uncertain significance |
| rs1193500324 | 9:136,444,440 | C/T | — | uncertain significance |
| rs1034593997 | 9:136,444,461 | G/A | — | uncertain significance |
| rs984921840 | 9:136,444,475 | G/A | — | uncertain significance |
| rs112395992 | 9:136,449,214 | C/T | — | — |
| rs371446639 | 9:136,449,913 | C/T | — | — |
| rs183489441 | 9:136,449,942 | G/A | — | — |
| rs113067637 | 9:136,452,411 | G/A | — | — |
| rs3025311 | 9:136,459,228 | A/G | intergenic variant | — |
| rs189525831 | 9:136,461,555 | G/T | intergenic variant | — |
| rs117522403 | 9:136,464,633 | G/A | intergenic variant | — |
| rs3888560 | 9:136,465,342 | G/T | — | — |
| rs78094364 | 9:136,466,679 | T/A | intergenic variant | — |
| rs577304144 | 9:136,466,728 | C/T | — | — |
| rs113927489 | 9:136,467,207 | C/G | intergenic variant | — |
| rs75596189 | 9:136,468,701 | C/T | regulatory region variant | — |
| rs62575398 | 9:136,468,866 | C/A | intergenic variant | — |
| rs56057809 | 9:136,472,460 | C/T | downstream gene variant | — |
| rs113864525 | 9:136,473,053 | C/A | downstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.