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rs920590

From SNPedia

Orientationplus
Stabilizedplus
Make rs920590(C;C)
Make rs920590(C;T)
Make rs920590(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position19793650
is asnp
is mentioned by
dbSNPrs920590
ebirs920590
HLIrs920590
Exacrs920590
Varsomers920590
Maprs920590
PheGenIrs920590
hapmaprs920590
1000 genomesrs920590
hgdprs920590
ensemblrs920590
gopubmedrs920590
geneviewrs920590
scholarrs920590
googlers920590
pharmgkbrs920590
gwascentralrs920590
openSNPrs920590
23andMers920590
23andMe allrs920590
SNP Nexus

SNPshotrs920590
SNPdbers920590
MSV3drs920590
GWAS Ctlgrs920590
GMAF0.3949
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22076464OA-icon.png]
Trait
Title Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia.
Risk Allele
P-val 0.000002
Odds Ratio None None