Rs10508343

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Orientationplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs10508343(A;A)
Make rs10508343(A;C)
ReferenceGRCh37 37.1/131
Chromosome10
Position8150713
is asnp
is mentioned by
dbSNPrs10508343
PheGenIrs10508343
nextbiors10508343
hapmaprs10508343
1000 genomesrs10508343
hgdprs10508343
ensemblrs10508343
gopubmedrs10508343
geneviewrs10508343
scholarrs10508343
googlers10508343
pharmgkbrs10508343
gwascentralrs10508343
openSNPrs10508343
23andMers10508343
23andMe allrs10508343
SNP Nexus

SNPshotrs10508343
SNPdbers10508343
MSV3drs10508343
GMAF0.0404
Max Magnitude0
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 19176441OA-icon.png]
Trait Treatment response for acute lymphoblastic leukemia
Title Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia
Risk Allele A
P-val 0.000008
Odds Ratio 3.81 [1.40-10.40]



GET Evidence
rs10508343
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.015625
summary