rs28940871(C;C)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs28940871 |
| Gene | HEXA |
| Chromosome | 15 |
| Position | 72,346,305 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| (C;G) | 3 | Carrier of a Tay-Sachs mutation |
| (G;G) | 5 | 23andMe = Tay-Sachs disease likely, but on other platforms this may be the normal form |
For 23andMe users, this is the normal genotype. However see also Rs28940871(G;G)
