rs587781335
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs587781335(C;G) |
Make rs587781335(G;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 16 |
Position | 68829754 |
Gene | CDH1 |
is a | snp |
is | mentioned by |
dbSNP | rs587781335 |
dbSNP (classic) | rs587781335 |
ClinGen | rs587781335 |
ebi | rs587781335 |
HLI | rs587781335 |
Exac | rs587781335 |
Gnomad | rs587781335 |
Varsome | rs587781335 |
LitVar | rs587781335 |
Map | rs587781335 |
PheGenI | rs587781335 |
Biobank | rs587781335 |
1000 genomes | rs587781335 |
hgdp | rs587781335 |
ensembl | rs587781335 |
geneview | rs587781335 |
scholar | rs587781335 |
rs587781335 | |
pharmgkb | rs587781335 |
gwascentral | rs587781335 |
openSNP | rs587781335 |
23andMe | rs587781335 |
SNPshot | rs587781335 |
SNPdbe | rs587781335 |
MSV3d | rs587781335 |
GWAS Ctlg | rs587781335 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587781335(G;G) |
Alt | rs587781335(G;G) |
Reference | Rs587781335(C;C) |
Significance | Unknown |
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.68863657C>G |
CLNSRC | |
CLNACC | RCV000129091.2, RCV000167901.1, |