rs138207610
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common/normal |
Make rs138207610(A;A) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 12 |
Position | 132676611 |
Gene | POLE |
is a | snp |
is | mentioned by |
dbSNP | rs138207610 |
dbSNP (classic) | rs138207610 |
ClinGen | rs138207610 |
ebi | rs138207610 |
HLI | rs138207610 |
Exac | rs138207610 |
Gnomad | rs138207610 |
Varsome | rs138207610 |
LitVar | rs138207610 |
Map | rs138207610 |
PheGenI | rs138207610 |
Biobank | rs138207610 |
1000 genomes | rs138207610 |
hgdp | rs138207610 |
ensembl | rs138207610 |
geneview | rs138207610 |
scholar | rs138207610 |
rs138207610 | |
pharmgkb | rs138207610 |
gwascentral | rs138207610 |
openSNP | rs138207610 |
23andMe | rs138207610 |
SNPshot | rs138207610 |
SNPdbe | rs138207610 |
MSV3d | rs138207610 |
GWAS Ctlg | rs138207610 |
Max Magnitude | 0 |
aka c.844C>T, p.Pro282Ser
Heterozygotes are predicted to have a significantly higher risk of colorectal cancer, based on both patient and theoretical studies.[PMID 23263490]