BNIP5
BCL2 interacting protein 5
Known Variants10 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|---|---|---|---|
| rs372892093 | 6:36,285,153 | T/C | — | likely benign |
| rs552447588 | 6:36,285,616 | G/A | — | — |
| rs193920980 | 6:36,291,094 | G/A | — | uncertain significance |
| rs9368922 | 6:36,295,976 | C/T | — | — |
| rs1463549134 | 6:36,296,386 | T/C | — | likely benign |
| rs41272160 | 6:36,297,893 | C/T | — | likely benign |
| rs761634583 | 6:36,298,002 | G/A | — | uncertain significance |
| rs758606753 | 6:36,298,070 | G/A | — | likely benign |
| rs201336652 | 6:36,298,275 | A/G | — | likely benign |
| rs2533288742 | 6:36,298,370 | T/C | — | uncertain significance |
Gene information from NCBI Gene. Variant classifications from ClinVar.