rs104894858(A;G)
From SNPedia
Familial hypertrophic cardiomyopathy (possible) |
Is a | genotype |
of | rs104894858 |
Gene | LAMP2 |
Chromosome | X |
Position | 120,442,599 |
mentioned | by |
Magnitude | 6 |
Repute | Bad |
Geno | Mag | Summary |
---|---|---|
(A;G) | 6 | Familial hypertrophic cardiomyopathy (possible) |
(G;G) | 0 | common in clinvar |
see discussion at rs104894858