rs143690372
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;T) | 7 | High risk of colorectal cancer |
(T;T) | 0 | common/normal |
Make rs143690372(C;C) |
Reference | GRCh38.p7 38.3/151 |
Chromosome | 12 |
Position | 132676616 |
Gene | POLE |
is a | snp |
is | mentioned by |
dbSNP | rs143690372 |
dbSNP (classic) | rs143690372 |
ClinGen | rs143690372 |
ebi | rs143690372 |
HLI | rs143690372 |
Exac | rs143690372 |
Gnomad | rs143690372 |
Varsome | rs143690372 |
LitVar | rs143690372 |
Map | rs143690372 |
PheGenI | rs143690372 |
Biobank | rs143690372 |
1000 genomes | rs143690372 |
hgdp | rs143690372 |
ensembl | rs143690372 |
geneview | rs143690372 |
scholar | rs143690372 |
rs143690372 | |
pharmgkb | rs143690372 |
gwascentral | rs143690372 |
openSNP | rs143690372 |
23andMe | rs143690372 |
SNPshot | rs143690372 |
SNPdbe | rs143690372 |
MSV3d | rs143690372 |
GWAS Ctlg | rs143690372 |
Max Magnitude | 7 |
aka c.839A>G, p.Lys280Arg
Heterozygotes are predicted to have a significantly higher risk of colorectal cancer, based on both patient and theoretical studies.[PMID 23263490]