rs587777374(A;G)

possible causal congenital heart defect mutation

Is a	genotype
of	rs587777374
Gene	NR2F2
Chromosome	15
Position	96,334,604
mentioned	by

Magnitude

6

Repute

Bad

Geno	Mag	Summary
(A;G)	6	possible causal congenital heart defect mutation
(G;G)	0	common in clinvar

see ClinVar links