rs16260
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 2.6x increased risk of prostate cancer | |
(A;C) | 1.5-1.7x increased risk of prostate cancer | |
(C;C) | 0 | normal |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 68737131 |
Gene | CDH1 |
is a | snp |
is | mentioned by |
dbSNP | rs16260 |
dbSNP (classic) | rs16260 |
ClinGen | rs16260 |
ebi | rs16260 |
HLI | rs16260 |
Exac | rs16260 |
Gnomad | rs16260 |
Varsome | rs16260 |
LitVar | rs16260 |
Map | rs16260 |
PheGenI | rs16260 |
Biobank | rs16260 |
1000 genomes | rs16260 |
hgdp | rs16260 |
ensembl | rs16260 |
geneview | rs16260 |
scholar | rs16260 |
rs16260 | |
pharmgkb | rs16260 |
gwascentral | rs16260 |
openSNP | rs16260 |
23andMe | rs16260 |
SNPshot | rs16260 |
SNPdbe | rs16260 |
MSV3d | rs16260 |
GWAS Ctlg | rs16260 |
GMAF | 0.2323 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 14961571, PMID 16189707] rs16260 (A) SNP located in the promoter region of the E-cadherin CDH1 gene is associated with increased risk of hereditary prostate cancer.
The effect appears to be additive, in that compared to the rs16260(C;C) homozygotes, the rs16260(A;C) heterozygotes are at about a 1.5 - 1.7 fold increased risk, and the rs16260(A;A) homozygotes are at about a 2.6 fold increased risk.
- see also OMIM 192090.0018
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ClinVar | |
---|---|
Risk | Rs16260(A;A) |
Alt | Rs16260(A;A) |
Reference | Rs16260(C;C) |
Significance | Other |
Disease | Prostate cancer |
Variation | info |
Gene | CDH1 |
CLNDBN | Prostate cancer, susceptibility to |
Reversed | 0 |
HGVS | NC_000016.9:g.68771034C>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000013034.3, |
[PMID 27852262] E-cadherin genetic variants predict survival outcome in breast cancer patients.