rs104894370(T;T)

common in clinvar

Is a	genotype
of	rs104894370
Gene	MYL2
Chromosome	12
Position	110,919,145
Merged from	Rs28932774
mentioned	by

Magnitude

0

Repute

Good

Geno	Mag	Summary
(C;T)	6.2	Familial Hypertrophic Cardiomyopathy
(T;T)	0	common in clinvar