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rs4366490

From SNPedia

Orientationplus
Stabilizedplus
Make rs4366490(C;C)
Make rs4366490(C;T)
Make rs4366490(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position63145382
GeneSLC22A24
is asnp
is mentioned by
dbSNPrs4366490
ebirs4366490
HLIrs4366490
Exacrs4366490
Varsomers4366490
Maprs4366490
PheGenIrs4366490
hapmaprs4366490
1000 genomesrs4366490
hgdprs4366490
ensemblrs4366490
gopubmedrs4366490
geneviewrs4366490
scholarrs4366490
googlers4366490
pharmgkbrs4366490
gwascentralrs4366490
openSNPrs4366490
23andMers4366490
23andMe allrs4366490
SNP Nexus

SNPshotrs4366490
SNPdbers4366490
MSV3drs4366490
GWAS Ctlgrs4366490
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 1E-6
Odds Ratio 1.70 [1.36-2.12]