FAM228A
family with sequence similarity 228 member A
Known Variants17 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs747210211 | 2:24,398,419 | C/A | — | uncertain significance |
| rs543111385 | 2:24,398,426 | C/T | — | uncertain significance |
| rs747128968 | 2:24,398,432 | C/G | — | uncertain significance |
| rs199513748 | 2:24,400,738 | A/G | — | uncertain significance |
| rs566611327 | 2:24,406,178 | C/T | — | uncertain significance |
| rs368889734 | 2:24,406,399 | G/C | — | uncertain significance |
| rs1377062257 | 2:24,406,434 | C/A | — | uncertain significance |
| rs369812559 | 2:24,406,436 | C/T | — | uncertain significance |
| rs2465336819 | 2:24,406,477 | G/T | — | uncertain significance |
| rs183368613 | 2:24,408,153 | G/A | intron variant | — |
| rs538215572 | 2:24,409,263 | A/G | — | — |
| rs56006260 | 2:24,409,903 | A/G | intron variant | — |
| rs2288073 | 2:24,413,298 | A/G | missense variant | — |
| rs1573811308 | 2:24,413,391 | A/G | — | likely benign |
| rs201826849 | 2:24,413,432 | G/T | — | uncertain significance |
| rs777963297 | 2:24,413,453 | G/T | — | uncertain significance |
| rs146891535 | 2:24,413,473 | C/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.