FAM219B
family with sequence similarity 219 member B
Known Variants23 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs1044086188 | 15:75,195,004 | A/G | — | uncertain significance |
| rs568406248 | 15:75,195,016 | T/C | — | likely benign |
| rs2505866083 | 15:75,195,025 | C/T | — | uncertain significance |
| rs780874223 | 15:75,195,028 | T/A | — | uncertain significance |
| rs2505866293 | 15:75,195,033 | T/G | — | uncertain significance |
| rs377053696 | 15:75,195,058 | C/T | — | uncertain significance |
| rs143038267 | 15:75,195,125 | C/G | — | uncertain significance |
| rs6495129 | 15:75,196,717 | G/T | downstream gene variant | — |
| rs997046876 | 15:75,197,501 | G/T | — | uncertain significance |
| rs775396439 | 15:75,197,532 | T/G | — | uncertain significance |
| rs766483154 | 15:75,197,568 | C/G | — | uncertain significance |
| rs772206811 | 15:75,198,653 | C/A | — | uncertain significance |
| rs2065207329 | 15:75,198,964 | T/C | — | uncertain significance |
| rs751347469 | 15:75,199,000 | G/A | — | uncertain significance |
| rs2505906967 | 15:75,199,003 | C/T | — | uncertain significance |
| rs1028906963 | 15:75,199,018 | C/T | — | uncertain significance |
| rs543038610 | 15:75,199,041 | G/A | — | uncertain significance |
| rs1331531485 | 15:75,199,081 | T/C | — | likely benign |
| rs1442147612 | 15:75,199,087 | G/A | — | uncertain significance |
| rs2505908676 | 15:75,199,114 | C/G | — | uncertain significance |
| rs1416706695 | 15:75,199,127 | C/A | — | uncertain significance |
| rs1316671958 | 15:75,199,128 | T/C | — | uncertain significance |
| rs183959177 | 15:75,200,161 | A/G | upstream gene variant | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.