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rs587777374

From SNPedia

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


Make rs587777374(A;A)
ReferenceGRCh38 38.1/142
Chromosome15
Position96334604
GeneNR2F2
is asnp
is mentioned by
dbSNPrs587777374
ebirs587777374
HLIrs587777374
Exacrs587777374
Varsomers587777374
Maprs587777374
PheGenIrs587777374
hapmaprs587777374
1000 genomesrs587777374
hgdprs587777374
ensemblrs587777374
gopubmedrs587777374
geneviewrs587777374
scholarrs587777374
googlers587777374
pharmgkbrs587777374
gwascentralrs587777374
openSNPrs587777374
23andMers587777374
23andMe allrs587777374
SNP Nexus

SNPshotrs587777374
SNPdbers587777374
MSV3drs587777374
GWAS Ctlgrs587777374
Max Magnitude6
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,