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rs104894728(A;A)

From SNPedia
common in clinvar
Is agenotype
ofrs104894728
GeneTNNI3
Chromosome19
Position55,151,898
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 0 common in clinvar
(A;G) 5 Familial hypertrophic cardiomyopathy, type 7
(G;G) 6 Familial hypertrophic cardiomyopathy, type 7