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rs104894074

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104894074(C;T)
Make rs104894074(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position11708467
GeneGATA4
is asnp
is mentioned by
dbSNPrs104894074
ebirs104894074
HLIrs104894074
Exacrs104894074
Varsomers104894074
Maprs104894074
PheGenIrs104894074
hapmaprs104894074
1000 genomesrs104894074
hgdprs104894074
ensemblrs104894074
gopubmedrs104894074
geneviewrs104894074
scholarrs104894074
googlers104894074
pharmgkbrs104894074
gwascentralrs104894074
openSNPrs104894074
23andMers104894074
23andMe allrs104894074
SNP Nexus

SNPshotrs104894074
SNPdbers104894074
MSV3drs104894074
GWAS Ctlgrs104894074
Max Magnitude0
OMIM600576
Desc
Variant0003
Relatedalso
ClinVar
Risk rs104894074(T;T)
Alt rs104894074(T;T)
Reference rs104894074(C;C)
Significance Pathogenic
Disease Atrial septal defect 2
Variation info
Gene GATA4
CLNDBN Atrial septal defect 2
Reversed 0
HGVS NC_000008.10:g.11565976C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000009598.2,