rs9378805

Orientation

plus

Stabilized

plus

Make rs9378805(A;A)

Make rs9378805(A;C)

Make rs9378805(C;C)

Reference

GRCh37 37.1/131

Chromosome

6

Position

417727

is a	snp
is	mentioned by
dbSNP	rs9378805
dbSNP (classic)	rs9378805
ClinGen	rs9378805
ebi	rs9378805
HLI	rs9378805
Exac	rs9378805
Gnomad	rs9378805
Varsome	rs9378805
LitVar	rs9378805
Map	rs9378805
PheGenI	rs9378805
Biobank	rs9378805
1000 genomes	rs9378805
hgdp	rs9378805
ensembl	rs9378805
geneview	rs9378805
scholar	rs9378805
google	rs9378805
pharmgkb	rs9378805
gwascentral	rs9378805
openSNP	rs9378805
23andMe	rs9378805
SNPshot	rs9378805
SNPdbe	rs9378805
MSV3d	rs9378805
GWAS Ctlg	rs9378805

GMAF

0.3306

Max Magnitude

0

?	(A;A) (A;C) (C;C)	28

news Slager and colleagues validated these in an independent sample of patients. The strongest association for chronic Lymphocytic Leukemia (CLL) was for rs735665 on 11q24, where the risk was 50 percent higher. This was closely followed by a 39 percent increased risk associated with rs9378805 on 6p25. Note: this is not a published paper - this is a report of a conference presentation.

OMIM	612558
Desc	LEUKEMIA, CHRONIC LYMPHOCYTIC SUSCEPTIBILITY TO, 4
Variant
Related	also

[PMID 20332261] Genetic Susceptibility Variants for Chronic Lymphocytic Leukemia

GWAS snp
PMID	[PMID 21131588]
Trait
Title	Genome-wide association study identifies a novel susceptibility locus at 6p21.3 among familial CLL
Risk Allele	C
P-val	0.000002
Odds Ratio	1.3800 [1.20-1.58]

[PMID 19619313] An assessment of the portability of ancestry informative markers between human populations.