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rs121917761(A;G)

From SNPedia

Familial restrictive cardiomyopathy, type 1 as a possibility
Is agenotype
ofrs121917761
GeneTNNI3
Chromosome19
Position55,154,068
mentionedby
Magnitude5
ReputeBad
Geno Mag Summary
(G;G) 0 common in clinvar

See discussion at rs121917761.