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rs10508343

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs10508343(A;A)
Make rs10508343(A;C)
ReferenceGRCh38 38.1/142
Chromosome10
Position8108750
is asnp
is mentioned by
dbSNPrs10508343
dbSNP (classic)rs10508343
ClinGenrs10508343
ebirs10508343
HLIrs10508343
Exacrs10508343
Gnomadrs10508343
Varsomers10508343
LitVarrs10508343
Maprs10508343
PheGenIrs10508343
Biobankrs10508343
1000 genomesrs10508343
hgdprs10508343
ensemblrs10508343
geneviewrs10508343
scholarrs10508343
googlers10508343
pharmgkbrs10508343
gwascentralrs10508343
openSNPrs10508343
23andMers10508343
SNPshotrs10508343
SNPdbers10508343
MSV3drs10508343
GWAS Ctlgrs10508343
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]