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rs104894858(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs104894858
GeneLAMP2
ChromosomeX
Position120,442,599
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;G) 6 Familial hypertrophic cardiomyopathy (possible)
(G;G) 0 common in clinvar