rs756198077
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs756198077(A;A) |
Make rs756198077(A;G) |
Make rs756198077(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 7 |
Position | 124842883 |
Gene | POT1 |
is a | snp |
is | mentioned by |
dbSNP | rs756198077 |
dbSNP (classic) | rs756198077 |
ClinGen | rs756198077 |
ebi | rs756198077 |
HLI | rs756198077 |
Exac | rs756198077 |
Gnomad | rs756198077 |
Varsome | rs756198077 |
LitVar | rs756198077 |
Map | rs756198077 |
PheGenI | rs756198077 |
Biobank | rs756198077 |
1000 genomes | rs756198077 |
hgdp | rs756198077 |
ensembl | rs756198077 |
geneview | rs756198077 |
scholar | rs756198077 |
rs756198077 | |
pharmgkb | rs756198077 |
gwascentral | rs756198077 |
openSNP | rs756198077 |
23andMe | rs756198077 |
SNPshot | rs756198077 |
SNPdbe | rs756198077 |
MSV3d | rs756198077 |
GWAS Ctlg | rs756198077 |
Max Magnitude | 0 |
rs756198077, also known as c.1087C>T and p.Arg363Ter, represents a rare mutation in the POT1 gene on chromosome 7.
Inherited dominantly, the minor allele is reported to increase risk for colorectal cancer. 10.1038/ncomms11883