rs786203576
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;G) | 5 | Hereditary cancer-predisposing syndrome; gastric cancer related? |
(G;G) | 0 | common in clinvar |
Make rs786203576(A;A) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 16 |
Position | 68738308 |
Gene | CDH1 |
is a | snp |
is | mentioned by |
dbSNP | rs786203576 |
dbSNP (classic) | rs786203576 |
ClinGen | rs786203576 |
ebi | rs786203576 |
HLI | rs786203576 |
Exac | rs786203576 |
Gnomad | rs786203576 |
Varsome | rs786203576 |
LitVar | rs786203576 |
Map | rs786203576 |
PheGenI | rs786203576 |
Biobank | rs786203576 |
1000 genomes | rs786203576 |
hgdp | rs786203576 |
ensembl | rs786203576 |
geneview | rs786203576 |
scholar | rs786203576 |
rs786203576 | |
pharmgkb | rs786203576 |
gwascentral | rs786203576 |
openSNP | rs786203576 |
23andMe | rs786203576 |
SNPshot | rs786203576 |
SNPdbe | rs786203576 |
MSV3d | rs786203576 |
GWAS Ctlg | rs786203576 |
Max Magnitude | 5 |
aka c.60G>A, p.Trp20Ter and W20X
ClinVar | |
---|---|
Risk | rs786203576(A;A) |
Alt | rs786203576(A;A) |
Reference | Rs786203576(G;G) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | CDH1 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000016.9:g.68772211G>A |
CLNSRC | |
CLNACC | RCV000166954.1, |