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rs397516406(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs397516406
GeneMYL2
Chromosome12
Position110,911,093
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;G) 6 Familial hypertrophic cardiomyopathy (possible)
(G;G) 0 common in clinvar