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rs6507874

From SNPedia

Orientationplus
Stabilizedplus
Make rs6507874(C;C)
Make rs6507874(C;T)
Make rs6507874(T;T)
ReferenceGRCh38 38.1/142
Chromosome18
Position48922435
GeneSMAD7
is asnp
is mentioned by
dbSNPrs6507874
dbSNP (classic)rs6507874
ClinGenrs6507874
ebirs6507874
HLIrs6507874
Exacrs6507874
Gnomadrs6507874
Varsomers6507874
LitVarrs6507874
Maprs6507874
PheGenIrs6507874
Biobankrs6507874
1000 genomesrs6507874
hgdprs6507874
ensemblrs6507874
geneviewrs6507874
scholarrs6507874
googlers6507874
pharmgkbrs6507874
gwascentralrs6507874
openSNPrs6507874
23andMers6507874
SNPshotrs6507874
SNPdbers6507874
MSV3drs6507874
GWAS Ctlgrs6507874
Max Magnitude0
? (C;C) (C;T) (T;T) 28


[PMID 25375357OA-icon.png] Multiple Functional Risk Variants in a SMAD7 Enhancer Implicate a Colorectal Cancer Risk Haplotype