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rs2059252

From SNPedia

Orientationplus
Stabilizedplus
Make rs2059252(A;A)
Make rs2059252(A;C)
Make rs2059252(C;C)
ReferenceGRCh38 38.1/141
Chromosome16
Position60698027
is asnp
is mentioned by
dbSNPrs2059252
ebirs2059252
HLIrs2059252
Exacrs2059252
Varsomers2059252
Maprs2059252
PheGenIrs2059252
hapmaprs2059252
1000 genomesrs2059252
hgdprs2059252
ensemblrs2059252
gopubmedrs2059252
geneviewrs2059252
scholarrs2059252
googlers2059252
pharmgkbrs2059252
gwascentralrs2059252
openSNPrs2059252
23andMers2059252
23andMe allrs2059252
SNP Nexus

SNPshotrs2059252
SNPdbers2059252
MSV3drs2059252
GWAS Ctlgrs2059252
GMAF0.05418
Max Magnitude

[PMID 22363440OA-icon.png] cis-Expression QTL Analysis of Established Colorectal Cancer Risk Variants in Colon Tumors and Adjacent Normal Tissue