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rs12150130

From SNPedia

Orientationplus
Stabilizedplus
Make rs12150130(C;C)
Make rs12150130(C;T)
Make rs12150130(T;T)
ReferenceGRCh38 38.1/142
Chromosome17
Position14213965
is asnp
is mentioned by
dbSNPrs12150130
ebirs12150130
HLIrs12150130
Exacrs12150130
Varsomers12150130
Maprs12150130
PheGenIrs12150130
hapmaprs12150130
1000 genomesrs12150130
hgdprs12150130
ensemblrs12150130
gopubmedrs12150130
geneviewrs12150130
scholarrs12150130
googlers12150130
pharmgkbrs12150130
gwascentralrs12150130
openSNPrs12150130
23andMers12150130
23andMe allrs12150130
SNP Nexus

SNPshotrs12150130
SNPdbers12150130
MSV3drs12150130
GWAS Ctlgrs12150130
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24800985OA-icon.png]
Trait Conotruncal heart defects
Title Genome-wide association study of maternal and inherited loci for conotruncal heart defects.
Risk Allele
P-val 6E-6
Odds Ratio 3.48 [1.96-6.21]