rs786201058
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
(G;T) | 5 | Hereditary cancer-predisposing syndrome; gastric cancer related? |
Make rs786201058(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 16 |
Position | 68738324 |
Gene | CDH1 |
is a | snp |
is | mentioned by |
dbSNP | rs786201058 |
dbSNP (classic) | rs786201058 |
ClinGen | rs786201058 |
ebi | rs786201058 |
HLI | rs786201058 |
Exac | rs786201058 |
Gnomad | rs786201058 |
Varsome | rs786201058 |
LitVar | rs786201058 |
Map | rs786201058 |
PheGenI | rs786201058 |
Biobank | rs786201058 |
1000 genomes | rs786201058 |
hgdp | rs786201058 |
ensembl | rs786201058 |
geneview | rs786201058 |
scholar | rs786201058 |
rs786201058 | |
pharmgkb | rs786201058 |
gwascentral | rs786201058 |
openSNP | rs786201058 |
23andMe | rs786201058 |
SNPshot | rs786201058 |
SNPdbe | rs786201058 |
MSV3d | rs786201058 |
GWAS Ctlg | rs786201058 |
Max Magnitude | 5 |
ClinVar | |
---|---|
Risk | rs786201058(C;C) rs786201058(T;T) |
Alt | rs786201058(C;C) rs786201058(T;T) |
Reference | Rs786201058(G;G) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome Hereditary diffuse gastric cancer |
Variation | info |
Gene | CDH1 |
CLNDBN | Hereditary cancer-predisposing syndrome Hereditary diffuse gastric cancer |
Reversed | 0 |
HGVS | NC_000016.9:g.68772227G>C; NC_000016.9:g.68772227G>T |
CLNSRC | |
CLNACC | RCV000223374.1, RCV000410130.1, RCV000162463.1, |