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rs2474937

From SNPedia

Orientationminus
Stabilizedminus
Make rs2474937(C;C)
Make rs2474937(C;T)
Make rs2474937(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position118360355
is asnp
is mentioned by
dbSNPrs2474937
ebirs2474937
HLIrs2474937
Exacrs2474937
Varsomers2474937
Maprs2474937
PheGenIrs2474937
hapmaprs2474937
1000 genomesrs2474937
hgdprs2474937
ensemblrs2474937
gopubmedrs2474937
geneviewrs2474937
scholarrs2474937
googlers2474937
pharmgkbrs2474937
gwascentralrs2474937
openSNPrs2474937
23andMers2474937
23andMe allrs2474937
SNP Nexus

SNPshotrs2474937
SNPdbers2474937
MSV3drs2474937
GWAS Ctlgrs2474937
GMAF0.2107
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23708190]
Trait Congenital heart malformation
Title A genome-wide association study identifies two risk loci for congenital heart malformations in Han Chinese populations.
Risk Allele C
P-val 8E-10
Odds Ratio 1.40 [1.26-1.56]


[PMID 25875170OA-icon.png] Association between the European GWAS-Identified Susceptibility Locus at Chromosome 4p16 and the Risk of Atrial Septal Defect: A Case-Control Study in Southwest China and a Meta-Analysis