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rs104894724(C;C)

From SNPedia

common in clinvar
Is agenotype
ofrs104894724
GeneTNNI3
Chromosome19
Position55,154,146
Merged fromRs28934871
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;G) 5 Familial hypertrophic cardiomyopathy, type 7
(C;T) 5 Familial restrictive cardiomyopathy, type 1
(G;G) 5 Familial hypertrophic cardiomyopathy, type 7
(T;T) 5 Familial restrictive cardiomyopathy, type 1