FAM227B
family with sequence similarity 227 member B
Known Variants40 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs776016532 | 15:49,620,872 | G/A | — | uncertain significance |
| rs2039542561 | 15:49,627,662 | T/G | — | uncertain significance |
| rs371011363 | 15:49,627,674 | G/A | — | uncertain significance |
| rs148287477 | 15:49,627,689 | G/A | — | uncertain significance |
| rs760640496 | 15:49,659,658 | T/C | — | uncertain significance |
| rs200556221 | 15:49,659,759 | T/C | — | uncertain significance |
| rs199971746 | 15:49,663,506 | G/T | — | uncertain significance |
| rs1232184760 | 15:49,663,561 | G/C | — | uncertain significance |
| rs2045795320 | 15:49,663,594 | T/C | — | uncertain significance |
| rs12909598 | 15:49,688,973 | G/A | — | — |
| rs36023246 | 15:49,699,311 | A/G | intron variant | — |
| rs35251997 | 15:49,706,145 | A/T | intron variant | — |
| rs73398276 | 15:49,710,979 | C/A | upstream gene variant | — |
| rs35698479 | 15:49,797,119 | A/G | intron variant | — |
| rs531301834 | 15:49,800,417 | T/C | — | uncertain significance |
| rs1360950724 | 15:49,800,476 | C/A | — | uncertain significance |
| rs571162637 | 15:49,800,477 | C/A | — | uncertain significance |
| rs62010017 | 15:49,817,864 | T/C | — | — |
| rs17402115 | 15:49,824,761 | C/T | intron variant | — |
| rs2543303623 | 15:49,833,927 | T/G | — | uncertain significance |
| rs371405816 | 15:49,833,942 | G/A | — | uncertain significance |
| rs2071095489 | 15:49,833,954 | G/A | — | uncertain significance |
| rs148925050 | 15:49,833,966 | G/A | — | uncertain significance |
| rs7182948 | 15:49,841,680 | A/C | — | — |
| rs566865466 | 15:49,842,251 | T/G | — | — |
| rs148166394 | 15:49,860,479 | A/G | — | uncertain significance |
| rs750848770 | 15:49,860,513 | C/A | — | uncertain significance |
| rs780889968 | 15:49,860,543 | G/C | — | uncertain significance |
| rs62021589 | 15:49,868,818 | T/C | — | — |
| rs919837777 | 15:49,868,982 | C/T | — | uncertain significance |
| rs771189627 | 15:49,869,015 | T/A | — | uncertain significance |
| rs12912703 | 15:49,869,141 | C/G | intron variant | — |
| rs139216008 | 15:49,869,854 | T/G | — | uncertain significance |
| rs7161744 | 15:49,872,347 | A/G | — | — |
| rs756487717 | 15:49,882,061 | G/C | — | uncertain significance |
| rs779619453 | 15:49,882,090 | C/T | — | uncertain significance |
| rs778713585 | 15:49,882,112 | A/C | — | uncertain significance |
| rs11632201 | 15:49,891,094 | T/C | intron variant | — |
| rs139422415 | 15:49,903,450 | G/A | — | uncertain significance |
| rs144125881 | 15:49,907,320 | C/T | — | likely benign |
Gene information from NCBI Gene. Variant classifications from ClinVar.