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rs11190164

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common/normal
Make rs11190164(A;G)
Make rs11190164(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome10
Position99591947
is asnp
is mentioned by
dbSNPrs11190164
dbSNP (old)rs11190164
ClinGenrs11190164
ebirs11190164
HLIrs11190164
Exacrs11190164
Gnomadrs11190164
Varsomers11190164
Maprs11190164
PheGenIrs11190164
Biobankrs11190164
1000 genomesrs11190164
hgdprs11190164
ensemblrs11190164
gopubmedrs11190164
geneviewrs11190164
scholarrs11190164
googlers11190164
pharmgkbrs11190164
gwascentralrs11190164
openSNPrs11190164
23andMers11190164
23andMe allrs11190164
SNPshotrs11190164
SNPdbers11190164
MSV3drs11190164
GWAS Ctlgrs11190164
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 29403313OA-icon.png] Strongly enhanced colorectal cancer risk stratification by combining family history and genetic risk score