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rs267759

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs267759(A;A)
Make rs267759(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position36137518
GeneLMBRD2
is asnp
is mentioned by
dbSNPrs267759
ebirs267759
HLIrs267759
Exacrs267759
Varsomers267759
Maprs267759
PheGenIrs267759
hapmaprs267759
1000 genomesrs267759
hgdprs267759
ensemblrs267759
gopubmedrs267759
geneviewrs267759
scholarrs267759
googlers267759
pharmgkbrs267759
gwascentralrs267759
openSNPrs267759
23andMers267759
23andMe allrs267759
SNP Nexus

SNPshotrs267759
SNPdbers267759
MSV3drs267759
GWAS Ctlgrs267759
GMAF0.1267
Max Magnitude0
? (A;A) (A;G) (G;G) 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 0.000007
Odds Ratio 3.23 [1.52-6.87]




GET Evidence
rs267759
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.882812
summary