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rs864321705

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864321705(G;G)
Make rs864321705(G;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position11755135
GeneGATA4
is asnp
is mentioned by
dbSNPrs864321705
ebirs864321705
HLIrs864321705
Exacrs864321705
Varsomers864321705
Maprs864321705
PheGenIrs864321705
hapmaprs864321705
1000 genomesrs864321705
hgdprs864321705
ensemblrs864321705
gopubmedrs864321705
geneviewrs864321705
scholarrs864321705
googlers864321705
pharmgkbrs864321705
gwascentralrs864321705
openSNPrs864321705
23andMers864321705
23andMe allrs864321705
SNP Nexus

SNPshotrs864321705
SNPdbers864321705
MSV3drs864321705
GWAS Ctlgrs864321705
Max Magnitude0
ClinVar
Risk rs864321705(G;G)
Alt rs864321705(G;G)
Reference rs864321705(T;T)
Significance Pathogenic
Disease Congenital heart disease
Variation info
Gene GATA4
CLNDBN Congenital heart disease
Reversed 0
HGVS NC_000008.10:g.11612644T>G
CLNSRC
CLNACC RCV000203595.1,