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rs9378805

From SNPedia

Orientationplus
Stabilizedplus
Make rs9378805(A;A)
Make rs9378805(A;C)
Make rs9378805(C;C)
ReferenceGRCh37 37.1/131
Chromosome6
Position417727
is asnp
is mentioned by
dbSNPrs9378805
ebirs9378805
HLIrs9378805
Exacrs9378805
Varsomers9378805
Maprs9378805
PheGenIrs9378805
hapmaprs9378805
1000 genomesrs9378805
hgdprs9378805
ensemblrs9378805
gopubmedrs9378805
geneviewrs9378805
scholarrs9378805
googlers9378805
pharmgkbrs9378805
gwascentralrs9378805
openSNPrs9378805
23andMers9378805
23andMe allrs9378805
SNP Nexus

SNPshotrs9378805
SNPdbers9378805
MSV3drs9378805
GWAS Ctlgrs9378805
GMAF0.3306
Max Magnitude
? (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.

OMIM612558
DescLEUKEMIA, CHRONIC LYMPHOCYTIC SUSCEPTIBILITY TO, 4
Variant
Relatedalso
[PMID 20332261OA-icon.png] Genetic Susceptibility Variants for Chronic Lymphocytic Leukemia
GWAS snp
PMID [PMID 21131588OA-icon.png]
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 19619313OA-icon.png] An assessment of the portability of ancestry informative markers between human populations.