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rs4762767

From SNPedia

Orientationminus
Stabilizedminus
Make rs4762767(C;C)
Make rs4762767(C;T)
Make rs4762767(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position19713195
is asnp
is mentioned by
dbSNPrs4762767
ebirs4762767
HLIrs4762767
Exacrs4762767
Varsomers4762767
Maprs4762767
PheGenIrs4762767
hapmaprs4762767
1000 genomesrs4762767
hgdprs4762767
ensemblrs4762767
gopubmedrs4762767
geneviewrs4762767
scholarrs4762767
googlers4762767
pharmgkbrs4762767
gwascentralrs4762767
openSNPrs4762767
23andMers4762767
23andMe allrs4762767
SNP Nexus

SNPshotrs4762767
SNPdbers4762767
MSV3drs4762767
GWAS Ctlgrs4762767
GMAF0.3274
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21946350OA-icon.png]
Trait
Title Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function.
Risk Allele G
P-val 0.000008
Odds Ratio 0.0270 [0.015-0.039] unit decrease