Rs17483466

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Orientationplus
is asnp
is mentioned by
dbSNPrs17483466
PheGenIrs17483466
nextbiors17483466
hapmaprs17483466
1000 genomesrs17483466
hgdprs17483466
ensemblrs17483466
gopubmedrs17483466
geneviewrs17483466
scholarrs17483466
googlers17483466
pharmgkbrs17483466
gwascentralrs17483466
openSNPrs17483466
23andMers17483466
23andMe allrs17483466
SNP Nexus

SNPshotrs17483466
SNPdbers17483466
MSV3drs17483466
GeneACOXL
Chromosome2
Orientationplus
GMAF0.118
Position111797458
ReferenceGRCh37 37.1/131
Max Magnitude
Make rs17483466(A;A)
Make rs17483466(A;G)
Make rs17483466(G;G)
? (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 20731705OA-icon.png] Genetic susceptibility for chronic lymphocytic leukemia among Chinese in Hong Kong.

GWAS snp
PMID [PMID 22700719OA-icon.png]
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


GET Evidence
rs17483466
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.103175
summary



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]