rs267606683(G;G)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs267606683 |
| Gene | SLC52A3 |
| Chromosome | 20 |
| Position | 765,564 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (A;A) | 8 | Brown-Vialetto-Van Laere syndrome type 1 mutation; riboflavin treatment recommended |
| (A;G) | 3 | Carrier of a Brown-Vialetto-Van Laere syndrome mutation |
| (G;G) | 0 | common in clinvar |
| (G;T) | 3 | Carrier of a Brown-Vialetto-Van Laere syndrome mutation |
| (T;T) | 8 | Brown-Vialetto-Van Laere Syndrome; riboflavin treatment recommended |
