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rs7156960

From SNPedia

Orientationplus
Stabilizedplus
Make rs7156960(C;C)
Make rs7156960(C;G)
Make rs7156960(G;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position76237008
is asnp
is mentioned by
dbSNPrs7156960
ebirs7156960
HLIrs7156960
Exacrs7156960
Varsomers7156960
Maprs7156960
PheGenIrs7156960
hapmaprs7156960
1000 genomesrs7156960
hgdprs7156960
ensemblrs7156960
gopubmedrs7156960
geneviewrs7156960
scholarrs7156960
googlers7156960
pharmgkbrs7156960
gwascentralrs7156960
openSNPrs7156960
23andMers7156960
23andMe allrs7156960
SNP Nexus

SNPshotrs7156960
SNPdbers7156960
MSV3drs7156960
GWAS Ctlgrs7156960
GMAF0.4467
Max Magnitude
? (C;C) (C;G) (G;G) 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 0.000001
Odds Ratio None None