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rs968451

From SNPedia

Orientationplus
Stabilizedplus
Make rs968451(G;G)
Make rs968451(G;T)
Make rs968451(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position39274846
is asnp
is mentioned by
dbSNPrs968451
ebirs968451
HLIrs968451
Exacrs968451
Varsomers968451
Maprs968451
PheGenIrs968451
hapmaprs968451
1000 genomesrs968451
hgdprs968451
ensemblrs968451
gopubmedrs968451
geneviewrs968451
scholarrs968451
googlers968451
pharmgkbrs968451
gwascentralrs968451
openSNPrs968451
23andMers968451
23andMe allrs968451
SNP Nexus

SNPshotrs968451
SNPdbers968451
MSV3drs968451
GWAS Ctlgrs968451
GMAF0.3274
Max Magnitude
? (G;G) (G;T) (T;T) 28
GWAS snp
PMID [PMID 21399635OA-icon.png]
Trait
Title Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis
Risk Allele T
P-val 1E-9
Odds Ratio 1.2700 [1.18-1.38]