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rs1365611

From SNPedia

Orientationplus
Stabilizedplus
Make rs1365611(C;C)
Make rs1365611(C;T)
Make rs1365611(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position174462542
is asnp
is mentioned by
dbSNPrs1365611
ebirs1365611
HLIrs1365611
Exacrs1365611
Varsomers1365611
Maprs1365611
PheGenIrs1365611
hapmaprs1365611
1000 genomesrs1365611
hgdprs1365611
ensemblrs1365611
gopubmedrs1365611
geneviewrs1365611
scholarrs1365611
googlers1365611
pharmgkbrs1365611
gwascentralrs1365611
openSNPrs1365611
23andMers1365611
23andMe allrs1365611
SNP Nexus

SNPshotrs1365611
SNPdbers1365611
MSV3drs1365611
GWAS Ctlgrs1365611
GMAF0.275
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 23717544OA-icon.png] Genetic Variation in 15-Hydroxyprostaglandin Dehydrogenase and Colon Cancer Susceptibility