rs11083846

Orientation

plus

Stabilized

plus

Make rs11083846(A;A)

Make rs11083846(A;G)

Make rs11083846(G;G)

Reference

GRCh38 38.1/141

Chromosome

19

Position

46704397

Gene

PRKD2

is a	snp
is	mentioned by
dbSNP	rs11083846
dbSNP (classic)	rs11083846
ClinGen	rs11083846
ebi	rs11083846
HLI	rs11083846
Exac	rs11083846
Gnomad	rs11083846
Varsome	rs11083846
LitVar	rs11083846
Map	rs11083846
PheGenI	rs11083846
Biobank	rs11083846
1000 genomes	rs11083846
hgdp	rs11083846
ensembl	rs11083846
geneview	rs11083846
scholar	rs11083846
google	rs11083846
pharmgkb	rs11083846
gwascentral	rs11083846
openSNP	rs11083846
23andMe	rs11083846
SNPshot	rs11083846
SNPdbe	rs11083846
MSV3d	rs11083846
GWAS Ctlg	rs11083846

GMAF

0.09963

Max Magnitude

0

?	(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 20332261] Genetic Susceptibility Variants for Chronic Lymphocytic Leukemia

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

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

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

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