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rs368489876

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs368489876(A;A)
Make rs368489876(A;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position11757012
GeneGATA4
is asnp
is mentioned by
dbSNPrs368489876
ebirs368489876
HLIrs368489876
Exacrs368489876
Varsomers368489876
Maprs368489876
PheGenIrs368489876
hapmaprs368489876
1000 genomesrs368489876
hgdprs368489876
ensemblrs368489876
gopubmedrs368489876
geneviewrs368489876
scholarrs368489876
googlers368489876
pharmgkbrs368489876
gwascentralrs368489876
openSNPrs368489876
23andMers368489876
23andMe allrs368489876
SNP Nexus

SNPshotrs368489876
SNPdbers368489876
MSV3drs368489876
GWAS Ctlgrs368489876
Max Magnitude0
ClinVar
Risk rs368489876(A;A)
Alt rs368489876(A;A)
Reference rs368489876(G;G)
Significance Pathogenic
Disease Ventricular septal defect 1
Variation info
Gene GATA4
CLNDBN Ventricular septal defect 1
Reversed 0
HGVS NC_000008.10:g.11614521G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000023006.4,