rs104894845(G;G)
From SNPedia
common in clinvar |
Is a | genotype |
of | rs104894845 |
Gene | GLA, RPL36A-HNRNPH2 |
Chromosome | X |
Position | 101,401,752 |
mentioned | by |
Magnitude | 0 |
Repute | Good |
Geno | Mag | Summary |
---|---|---|
(A;G) | 4 | Familial hypertrophic cardiomyopathy possible; but significance is uncertain |
(G;G) | 0 | common in clinvar |