FAM110D
family with sequence similarity 110 member D
Known Variants17 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs139482019 | 1:26,485,066 | G/A | upstream gene variant | — |
| rs768282431 | 1:26,487,817 | G/C | — | uncertain significance |
| rs752075305 | 1:26,487,882 | G/C | — | uncertain significance |
| rs375120944 | 1:26,487,982 | C/T | — | uncertain significance |
| rs1172401190 | 1:26,488,054 | G/A | — | uncertain significance |
| rs1470261116 | 1:26,488,176 | G/T | — | likely benign |
| rs1444483500 | 1:26,488,209 | C/G | — | uncertain significance |
| rs899131803 | 1:26,488,329 | C/G | — | uncertain significance |
| rs769436556 | 1:26,488,372 | C/G | — | uncertain significance |
| rs2523027461 | 1:26,488,386 | C/G | — | uncertain significance |
| rs763203514 | 1:26,488,398 | G/C | — | uncertain significance |
| rs767376935 | 1:26,488,422 | A/C | — | uncertain significance |
| rs1316008005 | 1:26,488,480 | C/T | — | uncertain significance |
| rs541850901 | 1:26,488,500 | C/T | — | uncertain significance |
| rs868633560 | 1:26,488,507 | C/T | — | uncertain significance |
| rs2523028216 | 1:26,488,519 | T/C | — | uncertain significance |
| rs1038261775 | 1:26,488,533 | C/T | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.