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rs496601

From SNPedia

Orientationplus
Stabilizedplus
Make rs496601(A;A)
Make rs496601(A;G)
Make rs496601(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position58863970
is asnp
is mentioned by
dbSNPrs496601
ebirs496601
HLIrs496601
Exacrs496601
Varsomers496601
Maprs496601
PheGenIrs496601
hapmaprs496601
1000 genomesrs496601
hgdprs496601
ensemblrs496601
gopubmedrs496601
geneviewrs496601
scholarrs496601
googlers496601
pharmgkbrs496601
gwascentralrs496601
openSNPrs496601
23andMers496601
23andMe allrs496601
SNP Nexus

SNPshotrs496601
SNPdbers496601
MSV3drs496601
GWAS Ctlgrs496601
GMAF0.1171
Max Magnitude

[PMID 24194259OA-icon.png] Racial differences in the association of insulin-like growth factor pathway and colorectal adenoma risk