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rs7578361

From SNPedia

Orientationplus
Stabilizedplus
Make rs7578361(G;G)
Make rs7578361(G;T)
Make rs7578361(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position149540704
is asnp
is mentioned by
dbSNPrs7578361
ebirs7578361
HLIrs7578361
Exacrs7578361
Varsomers7578361
Maprs7578361
PheGenIrs7578361
hapmaprs7578361
1000 genomesrs7578361
hgdprs7578361
ensemblrs7578361
gopubmedrs7578361
geneviewrs7578361
scholarrs7578361
googlers7578361
pharmgkbrs7578361
gwascentralrs7578361
openSNPrs7578361
23andMers7578361
23andMe allrs7578361
SNP Nexus

SNPshotrs7578361
SNPdbers7578361
MSV3drs7578361
GWAS Ctlgrs7578361
GMAF0.3375
Max Magnitude
? (G;G) (G;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 8E-6
Odds Ratio 1.40 [1.21-1.63]