rs104894639(A;G)
From SNPedia
Carrier of a Sanfilippo syndrome type A mutation |
Is a | genotype |
of | rs104894639 |
Gene | SGSH |
Chromosome | 17 |
Position | 80,210,622 |
mentioned | by |
Magnitude | 3 |
Repute | Bad |
Geno | Mag | Summary |
---|---|---|
(A;G) | 3 | Carrier of a Sanfilippo syndrome type A mutation |
(G;G) | 0 | common in clinvar |
Unaffected unless carrying another pathogenic SGSH gene mutation