rs980578884
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs980578884(A;A) |
Make rs980578884(A;G) |
Make rs980578884(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 12 |
Position | 132673217 |
Gene | POLE |
is a | snp |
is | mentioned by |
dbSNP | rs980578884 |
dbSNP (classic) | rs980578884 |
ClinGen | rs980578884 |
ebi | rs980578884 |
HLI | rs980578884 |
Exac | rs980578884 |
Gnomad | rs980578884 |
Varsome | rs980578884 |
LitVar | rs980578884 |
Map | rs980578884 |
PheGenI | rs980578884 |
Biobank | rs980578884 |
1000 genomes | rs980578884 |
hgdp | rs980578884 |
ensembl | rs980578884 |
geneview | rs980578884 |
scholar | rs980578884 |
rs980578884 | |
pharmgkb | rs980578884 |
gwascentral | rs980578884 |
openSNP | rs980578884 |
23andMe | rs980578884 |
SNPshot | rs980578884 |
SNPdbe | rs980578884 |
MSV3d | rs980578884 |
GWAS Ctlg | rs980578884 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs980578884(T;T) |
Alt | rs980578884(T;T) |
Reference | Rs980578884(C;C) |
Significance | Pathogenic |
Disease | Colorectal cancer |
Variation | info |
Gene | POLE |
CLNDBN | Colorectal cancer, susceptibility to, 12 |
Reversed | 0 |
HGVS | NC_000012.11:g.133249803C>T |
CLNSRC | |
CLNACC | RCV000417197.1, |