rs587777371(A;C)

possible causal congenital heart defect mutation

Is a	genotype
of	rs587777371
Gene	NR2F2
Chromosome	15
Position	96,337,399
mentioned	by

Magnitude

6

Repute

Bad

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

see ClinVar links