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rs864321698

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864321698(A;A)
Make rs864321698(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position11708335
GeneGATA4
is asnp
is mentioned by
dbSNPrs864321698
ebirs864321698
HLIrs864321698
Exacrs864321698
Varsomers864321698
Maprs864321698
PheGenIrs864321698
hapmaprs864321698
1000 genomesrs864321698
hgdprs864321698
ensemblrs864321698
gopubmedrs864321698
geneviewrs864321698
scholarrs864321698
googlers864321698
pharmgkbrs864321698
gwascentralrs864321698
openSNPrs864321698
23andMers864321698
23andMe allrs864321698
SNP Nexus

SNPshotrs864321698
SNPdbers864321698
MSV3drs864321698
GWAS Ctlgrs864321698
Max Magnitude0
ClinVar
Risk rs864321698(A;A)
Alt rs864321698(A;A)
Reference rs864321698(C;C)
Significance Pathogenic
Disease Congenital heart disease
Variation info
Gene GATA4
CLNDBN Congenital heart disease
Reversed 0
HGVS NC_000008.10:g.11565844C>A
CLNSRC
CLNACC RCV000203585.1,