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rs864321704

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864321704(C;T)
Make rs864321704(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position11758409
GeneGATA4
is asnp
is mentioned by
dbSNPrs864321704
dbSNP (classic)rs864321704
ClinGenrs864321704
ebirs864321704
HLIrs864321704
Exacrs864321704
Gnomadrs864321704
Varsomers864321704
LitVarrs864321704
Maprs864321704
PheGenIrs864321704
Biobankrs864321704
1000 genomesrs864321704
hgdprs864321704
ensemblrs864321704
geneviewrs864321704
scholarrs864321704
googlers864321704
pharmgkbrs864321704
gwascentralrs864321704
openSNPrs864321704
23andMers864321704
SNPshotrs864321704
SNPdbers864321704
MSV3drs864321704
GWAS Ctlgrs864321704
Max Magnitude0
ClinVar
Risk rs864321704(T;T)
Alt rs864321704(T;T)
Reference Rs864321704(C;C)
Significance Pathogenic
Disease Congenital heart disease
Variation info
Gene GATA4
CLNDBN Congenital heart disease
Reversed 0
HGVS NC_000008.10:g.11615918C>T
CLNSRC
CLNACC RCV000203588.1,