rs1064794037(GCGAT;GCGAT)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs1064794037 |
| Gene | VHL |
| Chromosome | 3 |
| Position | 10,149,805 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (-;GCGAT) | 7 | Von Hippel-Lindau syndrome mutation |
| (GCGAT;GCGAT) | 0 | common in clinvar |
