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rs387906772

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs387906772(A;G)
Make rs387906772(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position11755064
GeneGATA4
is asnp
is mentioned by
dbSNPrs387906772
ebirs387906772
HLIrs387906772
Exacrs387906772
Varsomers387906772
Maprs387906772
PheGenIrs387906772
hapmaprs387906772
1000 genomesrs387906772
hgdprs387906772
ensemblrs387906772
gopubmedrs387906772
geneviewrs387906772
scholarrs387906772
googlers387906772
pharmgkbrs387906772
gwascentralrs387906772
openSNPrs387906772
23andMers387906772
23andMe allrs387906772
SNP Nexus

SNPshotrs387906772
SNPdbers387906772
MSV3drs387906772
GWAS Ctlgrs387906772
Max Magnitude0
ClinVar
Risk rs387906772(G;G)
Alt rs387906772(G;G)
Reference rs387906772(A;A)
Significance Pathogenic
Disease Atrial septal defect 2
Variation info
Gene GATA4
CLNDBN Atrial septal defect 2
Reversed 0
HGVS NC_000008.10:g.11612573A>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000023014.2,