Have questions? Visit https://www.reddit.com/r/SNPedia

rs911263

From SNPedia

Orientationminus
Stabilizedminus
Make rs911263(A;A)
Make rs911263(A;G)
Make rs911263(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position68286876
GeneRAD51B
is asnp
is mentioned by
dbSNPrs911263
ClinGenrs911263
ebirs911263
HLIrs911263
Exacrs911263
Varsomers911263
Maprs911263
PheGenIrs911263
hapmaprs911263
1000 genomesrs911263
hgdprs911263
ensemblrs911263
gopubmedrs911263
geneviewrs911263
scholarrs911263
googlers911263
pharmgkbrs911263
gwascentralrs911263
openSNPrs911263
23andMers911263
23andMe allrs911263
SNP Nexus

SNPshotrs911263
SNPdbers911263
MSV3drs911263
GWAS Ctlgrs911263
GMAF0.3815
Max Magnitude
? (A;A) (A;G) (G;G) 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 2E-11
Odds Ratio 1.2900 [1.20-1.39]