FAM222B
family with sequence similarity 222 member B
Summary
Located in nucleoplasm. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants42 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1210660991 | 17:27,085,327 | C/G | — | likely benign |
| rs199981422 | 17:27,085,339 | G/A | — | benign |
| rs766268956 | 17:27,085,341 | G/A | — | uncertain significance |
| rs36029715 | 17:27,085,353 | C/T | — | benign |
| rs201607912 | 17:27,085,397 | C/T | — | conflicting classifications of pathogenicity |
| rs2544500194 | 17:27,085,442 | T/G | — | uncertain significance |
| rs767748553 | 17:27,085,457 | T/C | — | uncertain significance |
| rs762089934 | 17:27,085,503 | C/T | — | uncertain significance |
| rs756846462 | 17:27,085,545 | C/A | — | uncertain significance |
| rs370487622 | 17:27,085,640 | T/C | — | uncertain significance |
| rs764486649 | 17:27,085,691 | G/A | — | uncertain significance |
| rs753217058 | 17:27,085,727 | G/A | — | uncertain significance |
| rs763413670 | 17:27,085,791 | G/A | — | uncertain significance |
| rs898139397 | 17:27,085,944 | G/T | — | uncertain significance |
| rs369987412 | 17:27,085,974 | C/T | — | uncertain significance |
| rs773766356 | 17:27,085,982 | G/A | — | uncertain significance |
| rs767489400 | 17:27,086,052 | G/A | — | uncertain significance |
| rs753661690 | 17:27,086,078 | C/T | — | uncertain significance |
| rs376069619 | 17:27,086,172 | C/A | — | uncertain significance |
| rs2544518850 | 17:27,086,355 | A/C | — | uncertain significance |
| rs754249813 | 17:27,086,358 | C/T | — | uncertain significance |
| rs564764437 | 17:27,086,396 | T/A | — | uncertain significance |
| rs2544523077 | 17:27,086,544 | C/G | — | uncertain significance |
| rs2544523195 | 17:27,086,552 | C/T | — | uncertain significance |
| rs538977003 | 17:27,086,651 | G/C | — | uncertain significance |
| rs1247152952 | 17:27,086,661 | T/C | — | uncertain significance |
| rs201634356 | 17:27,086,730 | T/C | — | uncertain significance |
| rs908117978 | 17:27,093,679 | C/T | — | uncertain significance |
| rs902214963 | 17:27,098,899 | T/C | — | — |
| rs7212367 | 17:27,100,795 | G/C | — | — |
| rs7217547 | 17:27,106,872 | C/G | intron variant | — |
| rs12451790 | 17:27,112,000 | C/G | intron variant | — |
| rs113044547 | 17:27,119,067 | C/T | intron variant | — |
| rs184490258 | 17:27,128,253 | C/T | upstream gene variant | — |
| rs9907256 | 17:27,140,073 | G/T | — | — |
| rs9909979 | 17:27,140,147 | A/G | — | — |
| rs12938360 | 17:27,149,900 | T/C | intron variant | — |
| rs12946844 | 17:27,170,156 | C/G | — | — |
| rs28847895 | 17:27,172,520 | T/A | — | — |
| rs11650788 | 17:27,174,523 | T/C | — | — |
| rs9892942 | 17:27,178,761 | C/G | — | — |
| rs35033748 | 17:27,179,590 | T/C | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.