Rs13397985

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Orientationplus
is asnp
is mentioned by
dbSNPrs13397985
PheGenIrs13397985
nextbiors13397985
hapmaprs13397985
1000 genomesrs13397985
hgdprs13397985
ensemblrs13397985
gopubmedrs13397985
geneviewrs13397985
scholarrs13397985
googlers13397985
pharmgkbrs13397985
gwascentralrs13397985
openSNPrs13397985
23andMers13397985
23andMe allrs13397985
SNP Nexus

SNPshotrs13397985
SNPdbers13397985
MSV3drs13397985
GeneSP110, SP140
Chromosome2
Orientationplus
GMAF0.1139
Position231091223
ReferenceGRCh37.p2 37.2/134
Max Magnitude
Make rs13397985(G;G)
Make rs13397985(G;T)
Make rs13397985(T;T)
? (G;G) (G;T) (T;T) 28

23andMe blog chronic lymphocytic leukemia

  • rs13397985 G 1.41
GWAS
SNP rs13397985
PubMedID [PMID 18758461]
Condition Chronic lymphocytic leukemia
Gene SP140, SP110
Risk Allele G
pValue 6.00E-010
OR 1.41
95% CI 1.26-1.57



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


[PMID 19620980OA-icon.png] Genetic variants at 6p21.33 are associated with susceptibility to follicular lymphoma.


[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 2E-7
Odds Ratio 1.3900 None


GET Evidence
rs13397985
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.101562
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 1E-22
Odds Ratio 1.45 [NR]


[PMID 23455380] Risk of genome-wide association study-identified genetic variants for non-Hodgkin lymphoma in a Chinese population.