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rs12186641

From SNPedia

Orientationplus
Stabilizedplus
Make rs12186641(C;C)
Make rs12186641(C;T)
Make rs12186641(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position51868281
is asnp
is mentioned by
dbSNPrs12186641
ebirs12186641
HLIrs12186641
Exacrs12186641
Varsomers12186641
Maprs12186641
PheGenIrs12186641
hapmaprs12186641
1000 genomesrs12186641
hgdprs12186641
ensemblrs12186641
gopubmedrs12186641
geneviewrs12186641
scholarrs12186641
googlers12186641
pharmgkbrs12186641
gwascentralrs12186641
openSNPrs12186641
23andMers12186641
23andMe allrs12186641
SNP Nexus

SNPshotrs12186641
SNPdbers12186641
MSV3drs12186641
GWAS Ctlgrs12186641
GMAF0.04132
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23708191OA-icon.png]
Trait Congenital heart disease
Title Genome-wide association study of multiple congenital heart disease phenotypes identifies a susceptibility locus for atrial septal defect at chromosome 4p16.
Risk Allele
P-val 7E-6
Odds Ratio 1.68 [NR]