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rs121917761(G;G)

From SNPedia
common in clinvar
Is agenotype
ofrs121917761
GeneTNNI3
Chromosome19
Position55,154,068
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(A;A) 5 Familial restrictive cardiomyopathy, type 1, as a possibility
(A;G) 5 Familial restrictive cardiomyopathy, type 1 as a possibility
(G;G) 0 common in clinvar