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rs2901286

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs2901286(A;A)
Make rs2901286(A;C)
ReferenceGRCh38 38.1/142
Chromosome10
Position121141109
is asnp
is mentioned by
dbSNPrs2901286
ebirs2901286
HLIrs2901286
Exacrs2901286
Varsomers2901286
Maprs2901286
PheGenIrs2901286
hapmaprs2901286
1000 genomesrs2901286
hgdprs2901286
ensemblrs2901286
gopubmedrs2901286
geneviewrs2901286
scholarrs2901286
googlers2901286
pharmgkbrs2901286
gwascentralrs2901286
openSNPrs2901286
23andMers2901286
23andMe allrs2901286
SNP Nexus

SNPshotrs2901286
SNPdbers2901286
MSV3drs2901286
GWAS Ctlgrs2901286
GMAF0.06612
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 0.000004
Odds Ratio 4.66 [1.58-13.7]




GET Evidence
rs2901286
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0390625
summary