rs7944004

Orientation

plus

Stabilized

plus

Make rs7944004(G;G)

Make rs7944004(G;T)

Make rs7944004(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

2289922

is a	snp
is	mentioned by
dbSNP	rs7944004
dbSNP (classic)	rs7944004
ClinGen	rs7944004
ebi	rs7944004
HLI	rs7944004
Exac	rs7944004
Gnomad	rs7944004
Varsome	rs7944004
LitVar	rs7944004
Map	rs7944004
PheGenI	rs7944004
Biobank	rs7944004
1000 genomes	rs7944004
hgdp	rs7944004
ensembl	rs7944004
geneview	rs7944004
scholar	rs7944004
google	rs7944004
pharmgkb	rs7944004
gwascentral	rs7944004
openSNP	rs7944004
23andMe	rs7944004
SNPshot	rs7944004
SNPdbe	rs7944004
MSV3d	rs7944004
GWAS Ctlg	rs7944004

GMAF

0.3861

Max Magnitude

0

?	(G;G) (G;T) (T;T)	28

GWAS snp
PMID	[PMID 23770605]
Trait	Chronic lymphocytic leukemia
Title	Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.
Risk Allele	T
P-val	2E-10
Odds Ratio	1.20 [1.13-1.27]