Known Variants8 total
| rsid | Position (GRCh37) | Alleles | Class | ClinVar |
|---|
| rs254781 | 5:88,000,636 | C/T | intron variant | — |
| rs194225 | 5:88,001,186 | A/G | intron variant | — |
| rs640177 | 5:88,002,084 | T/A | intron variant | — |
| rs447801 | 5:88,002,653 | T/A | — | — |
| rs454214 | 5:88,003,403 | C/G | — | — |
| rs448809 | 5:88,005,828 | G/T | intron variant | — |
| rs10454905 | 5:88,010,133 | A/G | — | — |
| rs40504 | 5:88,011,139 | G/A | — | — |
Gene information from NCBI Gene. Variant classifications from ClinVar.