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rs397516456(C;C)

From SNPedia
common in clinvar
Is agenotype
ofrs397516456
GeneTNNT2
Chromosome1
Position201,365,298
mentionedby
Magnitude0
ReputeGood
Geno Mag Summary
(C;C) 0 common in clinvar
(C;T) 6.2 Familial Hypertrophic Cardiomyopathy

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