Have questions? Visit https://www.reddit.com/r/SNPedia

rs864321701

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs864321701(A;T)
Make rs864321701(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position11708709
GeneGATA4
is asnp
is mentioned by
dbSNPrs864321701
ebirs864321701
HLIrs864321701
Exacrs864321701
Varsomers864321701
Maprs864321701
PheGenIrs864321701
hapmaprs864321701
1000 genomesrs864321701
hgdprs864321701
ensemblrs864321701
gopubmedrs864321701
geneviewrs864321701
scholarrs864321701
googlers864321701
pharmgkbrs864321701
gwascentralrs864321701
openSNPrs864321701
23andMers864321701
23andMe allrs864321701
SNP Nexus

SNPshotrs864321701
SNPdbers864321701
MSV3drs864321701
GWAS Ctlgrs864321701
Max Magnitude0
ClinVar
Risk rs864321701(T;T)
Alt rs864321701(T;T)
Reference rs864321701(A;A)
Significance Pathogenic
Disease Congenital heart disease
Variation info
Gene GATA4
CLNDBN Congenital heart disease
Reversed 0
HGVS NC_000008.10:g.11566218A>T
CLNSRC
CLNACC RCV000203586.1,