rs864622655
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;A) | 6.7 | CDH1-based gastric cancer risk |
(A;A) | 0 | common in clinvar |
Make rs864622655(-;-) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 16 |
Position | 68808540 |
Gene | CDH1 |
is a | snp |
is | mentioned by |
dbSNP | rs864622655 |
dbSNP (classic) | rs864622655 |
ClinGen | rs864622655 |
ebi | rs864622655 |
HLI | rs864622655 |
Exac | rs864622655 |
Gnomad | rs864622655 |
Varsome | rs864622655 |
LitVar | rs864622655 |
Map | rs864622655 |
PheGenI | rs864622655 |
Biobank | rs864622655 |
1000 genomes | rs864622655 |
hgdp | rs864622655 |
ensembl | rs864622655 |
geneview | rs864622655 |
scholar | rs864622655 |
rs864622655 | |
pharmgkb | rs864622655 |
gwascentral | rs864622655 |
openSNP | rs864622655 |
23andMe | rs864622655 |
SNPshot | rs864622655 |
SNPdbe | rs864622655 |
MSV3d | rs864622655 |
GWAS Ctlg | rs864622655 |
Max Magnitude | 6.7 |
Also known as c.504delA, the minor allele is considered a pathogenic rare mutation for hereditary diffuse gastric cancer in ClinVar.
ClinVar | |
---|---|
Risk | rs864622655(-;-) |
Alt | rs864622655(-;-) |
Reference | Rs864622655(A;A) |
Significance | Pathogenic |
Disease | Hereditary diffuse gastric cancer |
Variation | info |
Gene | CDH1 |
CLNDBN | Hereditary diffuse gastric cancer |
Reversed | 0 |
HGVS | NC_000016.9:g.68842443delA |
CLNSRC | |
CLNACC | RCV000204728.2, |