rs17483466

Orientation

plus

Stabilized

plus

Make rs17483466(A;A)

Make rs17483466(A;G)

Make rs17483466(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

111039881

Gene

ACOXL

is a	snp
is	mentioned by
dbSNP	rs17483466
dbSNP (classic)	rs17483466
ClinGen	rs17483466
ebi	rs17483466
HLI	rs17483466
Exac	rs17483466
Gnomad	rs17483466
Varsome	rs17483466
LitVar	rs17483466
Map	rs17483466
PheGenI	rs17483466
Biobank	rs17483466
1000 genomes	rs17483466
hgdp	rs17483466
ensembl	rs17483466
geneview	rs17483466
scholar	rs17483466
google	rs17483466
pharmgkb	rs17483466
gwascentral	rs17483466
openSNP	rs17483466
23andMe	rs17483466
SNPshot	rs17483466
SNPdbe	rs17483466
MSV3d	rs17483466
GWAS Ctlg	rs17483466

GMAF

0.118

Max Magnitude

0

?	(A;A) (A;G) (G;G)	28

23andMe blog chronic lymphocytic leukemia

• rs17483466 G 1.39

GWAS
SNP	rs17483466
PubMedID	[PMID 18758461]
Condition	Chronic lymphocytic leukemia
Gene	ACOXL,BCL2L11
Risk Allele	G
pValue	2.00E-010
OR	1.39
95% CI	1.25-1.53

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

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

GWAS snp
PMID	[PMID 22700719]
Trait
Title	Common variation at 6p21.31 (BAK1) influences the risk of chronic lymphocytic leukemia.
Risk Allele
P-val	5E-9
Odds Ratio	1.4300 None

GWAS snp
PMID	[PMID 23770605]
Trait	Chronic lymphocytic leukemia
Title	Genome-wide association study identifies multiple risk loci for chronic lymphocytic leukemia.
Risk Allele	G
P-val	4E-17
Odds Ratio	1.37 [NR]