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

rs864321703

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864321703(A;A)
Make rs864321703(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position11708339
GeneGATA4
is asnp
is mentioned by
dbSNPrs864321703
ebirs864321703
HLIrs864321703
Exacrs864321703
Varsomers864321703
Maprs864321703
PheGenIrs864321703
hapmaprs864321703
1000 genomesrs864321703
hgdprs864321703
ensemblrs864321703
gopubmedrs864321703
geneviewrs864321703
scholarrs864321703
googlers864321703
pharmgkbrs864321703
gwascentralrs864321703
openSNPrs864321703
23andMers864321703
23andMe allrs864321703
SNP Nexus

SNPshotrs864321703
SNPdbers864321703
MSV3drs864321703
GWAS Ctlgrs864321703
Max Magnitude0
ClinVar
Risk rs864321703(A;A)
Alt rs864321703(A;A)
Reference rs864321703(C;C)
Significance Pathogenic
Disease Congenital heart disease
Variation info
Gene GATA4
CLNDBN Congenital heart disease
Reversed 0
HGVS NC_000008.10:g.11565848C>A
CLNSRC
CLNACC RCV000203605.1,