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rs11083846

From SNPedia

Orientationplus
Stabilizedplus
Make rs11083846(A;A)
Make rs11083846(A;G)
Make rs11083846(G;G)
ReferenceGRCh38 38.1/141
Chromosome19
Position46704397
GenePRKD2
is asnp
is mentioned by
dbSNPrs11083846
ebirs11083846
HLIrs11083846
Exacrs11083846
Varsomers11083846
Maprs11083846
PheGenIrs11083846
hapmaprs11083846
1000 genomesrs11083846
hgdprs11083846
ensemblrs11083846
gopubmedrs11083846
geneviewrs11083846
scholarrs11083846
googlers11083846
pharmgkbrs11083846
gwascentralrs11083846
openSNPrs11083846
23andMers11083846
23andMe allrs11083846
SNP Nexus

SNPshotrs11083846
SNPdbers11083846
MSV3drs11083846
GWAS Ctlgrs11083846
GMAF0.09963
Max Magnitude
? (A;A) (A;G) (G;G) 28

23andMe blog chronic lymphocytic leukemia

  • rs11083846 A 1.35
GWAS snp
PMID [PMID 18758461]
Trait Chronic lymphocytic leukemia
Title A genome-wide association study identifies six susceptibility loci for chronic lymphocytic leukemia
Risk Allele A
P-val 4.0000000000000002E-9
Odds Ratio 1.35 [1.22-1.49]


[PMID 20332261OA-icon.png] Genetic Susceptibility Variants for Chronic Lymphocytic Leukemia


[PMID 20855867] Inherited genetic susceptibility to monoclonal B-cell lymphocytosis


[PMID 20369022OA-icon.png] Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations.


[PMID 20731705OA-icon.png] Genetic susceptibility for chronic lymphocytic leukemia among Chinese in Hong Kong.


GET Evidence
rs11083846
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.183305
summary



[PMID 23455380] Risk of genome-wide association study-identified genetic variants for non-Hodgkin lymphoma in a Chinese population.