FAM193B
family with sequence similarity 193 member B
Summary
Located in cytoplasm; nuclear speck; and nucleolus. [provided by Alliance of Genome Resources, Jul 2025]
Known Variants53 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs2532120954 | 5:176,948,986 | G/A | — | uncertain significance |
| rs770654965 | 5:176,948,989 | C/T | — | uncertain significance |
| rs371661866 | 5:176,951,227 | C/T | — | uncertain significance |
| rs1360810861 | 5:176,951,257 | T/C | — | uncertain significance |
| rs563536004 | 5:176,951,401 | C/T | — | uncertain significance |
| rs1396847941 | 5:176,951,411 | C/T | — | uncertain significance |
| rs1315059468 | 5:176,951,413 | C/T | — | uncertain significance |
| rs750861205 | 5:176,951,477 | C/T | — | uncertain significance |
| rs369935019 | 5:176,951,521 | C/T | — | likely benign |
| rs1264367735 | 5:176,951,524 | G/A | — | uncertain significance |
| rs775210849 | 5:176,951,561 | C/T | — | uncertain significance |
| rs374096273 | 5:176,951,698 | C/T | — | uncertain significance |
| rs192898913 | 5:176,951,707 | T/C | missense variant | — |
| rs767944740 | 5:176,951,756 | C/T | — | uncertain significance |
| rs1381716969 | 5:176,951,765 | G/A | — | uncertain significance |
| rs201707860 | 5:176,952,023 | G/A | — | uncertain significance |
| rs200390629 | 5:176,952,085 | C/T | — | uncertain significance |
| rs1051319121 | 5:176,952,086 | G/A | — | uncertain significance |
| rs376802512 | 5:176,952,089 | C/T | — | uncertain significance |
| rs571256081 | 5:176,952,142 | C/T | — | likely benign |
| rs370113154 | 5:176,952,158 | G/A | — | uncertain significance |
| rs982518885 | 5:176,959,505 | G/A | — | uncertain significance |
| rs370939557 | 5:176,959,591 | C/G | — | uncertain significance |
| rs768405345 | 5:176,959,602 | G/T | — | uncertain significance |
| rs377692481 | 5:176,959,631 | C/T | — | uncertain significance |
| rs376275999 | 5:176,963,392 | G/A | — | uncertain significance |
| rs2532283971 | 5:176,963,426 | A/G | — | uncertain significance |
| rs1256374895 | 5:176,963,440 | G/A | — | uncertain significance |
| rs1764173365 | 5:176,963,449 | C/T | — | uncertain significance |
| rs747801721 | 5:176,963,461 | G/A | — | uncertain significance |
| rs776616348 | 5:176,963,503 | T/C | — | uncertain significance |
| rs1409883292 | 5:176,963,548 | G/C | — | uncertain significance |
| rs368465178 | 5:176,963,590 | G/A | — | uncertain significance |
| rs747521855 | 5:176,963,609 | G/A | — | uncertain significance |
| rs371866393 | 5:176,963,626 | C/G | — | uncertain significance |
| rs1349786400 | 5:176,963,634 | G/T | — | uncertain significance |
| rs767383352 | 5:176,963,666 | G/C | — | uncertain significance |
| rs538182772 | 5:176,963,670 | G/C | — | uncertain significance |
| rs780445851 | 5:176,963,678 | C/T | — | uncertain significance |
| rs1466519908 | 5:176,963,686 | C/A | — | uncertain significance |
| rs187770859 | 5:176,964,165 | G/A | intron variant | — |
| rs750651608 | 5:176,964,892 | T/A | — | uncertain significance |
| rs377666621 | 5:176,964,916 | C/A | — | uncertain significance |
| rs746837825 | 5:176,964,948 | G/A | — | uncertain significance |
| rs369854968 | 5:176,964,960 | G/A | — | uncertain significance |
| rs200354448 | 5:176,965,939 | A/C | missense variant | — |
| rs2532318233 | 5:176,965,947 | C/T | — | uncertain significance |
| rs1453364299 | 5:176,965,974 | C/T | — | uncertain significance |
| rs970766637 | 5:176,966,028 | G/A | — | uncertain significance |
| rs758308940 | 5:176,981,269 | T/C | — | uncertain significance |
| rs533041891 | 5:176,981,273 | G/C | — | uncertain significance |
| rs975773856 | 5:176,981,401 | G/A | — | uncertain significance |
| rs2127499629 | 5:176,981,453 | G/A | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.