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rs11636802

From SNPedia

Orientationplus
Stabilizedplus
Make rs11636802(A;A)
Make rs11636802(A;G)
Make rs11636802(G;G)
ReferenceGRCh38 38.1/141
Chromosome15
Position56483399
is asnp
is mentioned by
dbSNPrs11636802
ebirs11636802
HLIrs11636802
Exacrs11636802
Varsomers11636802
Maprs11636802
PheGenIrs11636802
hapmaprs11636802
1000 genomesrs11636802
hgdprs11636802
ensemblrs11636802
gopubmedrs11636802
geneviewrs11636802
scholarrs11636802
googlers11636802
pharmgkbrs11636802
gwascentralrs11636802
openSNPrs11636802
23andMers11636802
23andMe allrs11636802
SNP Nexus

SNPshotrs11636802
SNPdbers11636802
MSV3drs11636802
GWAS Ctlgrs11636802
GMAF0.06566
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23770605OA-icon.png]
Trait Chronic lymphocytic leukemia
Title Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.
Risk Allele G
P-val 2E-13
Odds Ratio 1.41 [NR]