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rs1496766

From SNPedia

Orientationplus
Stabilizedplus
Make rs1496766(C;C)
Make rs1496766(C;T)
Make rs1496766(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position78702149
GeneMAGI2
is asnp
is mentioned by
dbSNPrs1496766
ebirs1496766
HLIrs1496766
Exacrs1496766
Varsomers1496766
Maprs1496766
PheGenIrs1496766
hapmaprs1496766
1000 genomesrs1496766
hgdprs1496766
ensemblrs1496766
gopubmedrs1496766
geneviewrs1496766
scholarrs1496766
googlers1496766
pharmgkbrs1496766
gwascentralrs1496766
openSNPrs1496766
23andMers1496766
23andMe allrs1496766
SNP Nexus

SNPshotrs1496766
SNPdbers1496766
MSV3drs1496766
GWAS Ctlgrs1496766
GMAF0.03949
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23007406OA-icon.png]
Trait Acute lymphoblastic leukemia (childhood)
Title Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia.
Risk Allele C
P-val 5E-6
Odds Ratio 2.84 [1.81-4.44]