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rs3729856

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs3729856(A;G)
Make rs3729856(G;G)
ReferenceGRCh38 38.1/142
Chromosome8
Position11757066
GeneGATA4
is asnp
is mentioned by
dbSNPrs3729856
ebirs3729856
HLIrs3729856
Exacrs3729856
Varsomers3729856
Maprs3729856
PheGenIrs3729856
hapmaprs3729856
1000 genomesrs3729856
hgdprs3729856
ensemblrs3729856
gopubmedrs3729856
geneviewrs3729856
scholarrs3729856
googlers3729856
pharmgkbrs3729856
gwascentralrs3729856
openSNPrs3729856
23andMers3729856
23andMe allrs3729856
SNP Nexus

SNPshotrs3729856
SNPdbers3729856
MSV3drs3729856
GWAS Ctlgrs3729856
Max Magnitude0
? (A;A) (A;G) (G;G) 28
ClinVar
Risk rs3729856(G;G)
Alt rs3729856(G;G)
Reference rs3729856(A;A)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene GATA4
CLNDBN not specified not provided
Reversed 0
HGVS NC_000008.10:g.11614575A>G
CLNSRC ClinVar
CLNACC RCV000037322.2, RCV000128527.1,