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rs864321699

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs864321699(A;A)
Make rs864321699(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position11708337
GeneGATA4
is asnp
is mentioned by
dbSNPrs864321699
ebirs864321699
HLIrs864321699
Exacrs864321699
Varsomers864321699
Maprs864321699
PheGenIrs864321699
hapmaprs864321699
1000 genomesrs864321699
hgdprs864321699
ensemblrs864321699
gopubmedrs864321699
geneviewrs864321699
scholarrs864321699
googlers864321699
pharmgkbrs864321699
gwascentralrs864321699
openSNPrs864321699
23andMers864321699
23andMe allrs864321699
SNP Nexus

SNPshotrs864321699
SNPdbers864321699
MSV3drs864321699
GWAS Ctlgrs864321699
Max Magnitude0
ClinVar
Risk rs864321699(A;A)
Alt rs864321699(A;A)
Reference rs864321699(G;G)
Significance Pathogenic
Disease Congenital heart disease
Variation info
Gene GATA4
CLNDBN Congenital heart disease
Reversed 0
HGVS NC_000008.10:g.11565846G>A
CLNSRC
CLNACC RCV000203597.1,