rs6507875
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs6507875(C;C) |
Make rs6507875(C;G) |
Make rs6507875(G;G) |
Reference | GRCh38 38.1/142 |
Chromosome | 18 |
Position | 48922449 |
Gene | SMAD7 |
is a | snp |
is | mentioned by |
dbSNP | rs6507875 |
dbSNP (classic) | rs6507875 |
ClinGen | rs6507875 |
ebi | rs6507875 |
HLI | rs6507875 |
Exac | rs6507875 |
Gnomad | rs6507875 |
Varsome | rs6507875 |
LitVar | rs6507875 |
Map | rs6507875 |
PheGenI | rs6507875 |
Biobank | rs6507875 |
1000 genomes | rs6507875 |
hgdp | rs6507875 |
ensembl | rs6507875 |
geneview | rs6507875 |
scholar | rs6507875 |
rs6507875 | |
pharmgkb | rs6507875 |
gwascentral | rs6507875 |
openSNP | rs6507875 |
23andMe | rs6507875 |
SNPshot | rs6507875 |
SNPdbe | rs6507875 |
MSV3d | rs6507875 |
GWAS Ctlg | rs6507875 |
Max Magnitude | 0 |
[PMID 25375357] Multiple Functional Risk Variants in a SMAD7 Enhancer Implicate a Colorectal Cancer Risk Haplotype