rs587782359
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;T) | 5 | Hereditary cancer-predisposing syndrome; gastric cancer related? |
Make rs587782359(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 16 |
Position | 68812244 |
Gene | CDH1 |
is a | snp |
is | mentioned by |
dbSNP | rs587782359 |
dbSNP (classic) | rs587782359 |
ClinGen | rs587782359 |
ebi | rs587782359 |
HLI | rs587782359 |
Exac | rs587782359 |
Gnomad | rs587782359 |
Varsome | rs587782359 |
LitVar | rs587782359 |
Map | rs587782359 |
PheGenI | rs587782359 |
Biobank | rs587782359 |
1000 genomes | rs587782359 |
hgdp | rs587782359 |
ensembl | rs587782359 |
geneview | rs587782359 |
scholar | rs587782359 |
rs587782359 | |
pharmgkb | rs587782359 |
gwascentral | rs587782359 |
openSNP | rs587782359 |
23andMe | rs587782359 |
SNPshot | rs587782359 |
SNPdbe | rs587782359 |
MSV3d | rs587782359 |
GWAS Ctlg | rs587782359 |
Max Magnitude | 5 |
ClinVar | |
---|---|
Risk | rs587782359(G;G) rs587782359(T;T) |
Alt | rs587782359(G;G) rs587782359(T;T) |
Reference | Rs587782359(C;C) |
Significance | Probable-Pathogenic |
Disease | not specified Hereditary cancer-predisposing syndrome Hereditary diffuse gastric cancer |
Variation | info |
Gene | CDH1 |
CLNDBN | not specified Hereditary cancer-predisposing syndrome Hereditary diffuse gastric cancer |
Reversed | 0 |
HGVS | NC_000016.9:g.68846147C>G; NC_000016.9:g.68846147C>T |
CLNSRC | |
CLNACC | RCV000478907.1, RCV000131314.2, RCV000231218.1, RCV000481162.1, |