rs876660771
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 6.7 | CDH1-based gastric cancer risk |
Make rs876660771(A;A) |
Chromosome | 16 |
Position | 68812264 |
Gene | CDH1 |
is a | snp |
is | mentioned by |
dbSNP | rs876660771 |
dbSNP (classic) | rs876660771 |
ClinGen | rs876660771 |
ebi | rs876660771 |
HLI | rs876660771 |
Exac | rs876660771 |
Gnomad | rs876660771 |
Varsome | rs876660771 |
LitVar | rs876660771 |
Map | rs876660771 |
PheGenI | rs876660771 |
Biobank | rs876660771 |
1000 genomes | rs876660771 |
hgdp | rs876660771 |
ensembl | rs876660771 |
geneview | rs876660771 |
scholar | rs876660771 |
rs876660771 | |
pharmgkb | rs876660771 |
gwascentral | rs876660771 |
openSNP | rs876660771 |
23andMe | rs876660771 |
SNPshot | rs876660771 |
SNPdbe | rs876660771 |
MSV3d | rs876660771 |
GWAS Ctlg | rs876660771 |
Max Magnitude | 6.7 |
Also known as c.1137+1G>A, the minor allele is considered a pathogenic rare mutation for hereditary diffuse gastric cancer in ClinVar.
ClinVar | |
---|---|
Risk | rs876660771(A;A) |
Alt | rs876660771(A;A) |
Reference | Rs876660771(G;G) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome Hereditary diffuse gastric cancer not provided |
Variation | info |
Gene | CDH1 |
CLNDBN | Hereditary cancer-predisposing syndrome Hereditary diffuse gastric cancer not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.68846167G>A |
CLNSRC | |
CLNACC | RCV000219632.1, RCV000230827.2, RCV000483444.1, |