rs587777374

Orientation

plus

Stabilized

plus

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

Make rs587777374(A;A)

Reference

GRCh38 38.1/142

Chromosome

15

Position

96334604

Gene

NR2F2

is a	snp
is	mentioned by
dbSNP	rs587777374
dbSNP (classic)	rs587777374
ClinGen	rs587777374
ebi	rs587777374
HLI	rs587777374
Exac	rs587777374
Gnomad	rs587777374
Varsome	rs587777374
LitVar	rs587777374
Map	rs587777374
PheGenI	rs587777374
Biobank	rs587777374
1000 genomes	rs587777374
hgdp	rs587777374
ensembl	rs587777374
geneview	rs587777374
scholar	rs587777374
google	rs587777374
pharmgkb	rs587777374
gwascentral	rs587777374
openSNP	rs587777374
23andMe	rs587777374
SNPshot	rs587777374
SNPdbe	rs587777374
MSV3d	rs587777374
GWAS Ctlg	rs587777374

Max Magnitude

6

ClinVar
Risk	rs587777374(A;A)
Alt	rs587777374(A;A)
Reference	Rs587777374(G;G)
Significance	Pathogenic
Disease	Congenital heart defects
Variation	info
Gene	NR2F2
CLNDBN	Congenital heart defects, multiple types, 4
Reversed	0
HGVS	NC_000015.9:g.96877833G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000116202.4,