rs786204165
From SNPedia
Merged into | rs587781276 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(TG;TG) | 0 | common in clinvar |
Make rs786204165(-;-) |
Make rs786204165(-;TG) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 16 |
Position | 68823524 |
Gene | CDH1 |
is a | snp |
is | mentioned by |
dbSNP | rs786204165 |
dbSNP (classic) | rs786204165 |
ClinGen | rs786204165 |
ebi | rs786204165 |
HLI | rs786204165 |
Exac | rs786204165 |
Gnomad | rs786204165 |
Varsome | rs786204165 |
LitVar | rs786204165 |
Map | rs786204165 |
PheGenI | rs786204165 |
Biobank | rs786204165 |
1000 genomes | rs786204165 |
hgdp | rs786204165 |
ensembl | rs786204165 |
geneview | rs786204165 |
scholar | rs786204165 |
rs786204165 | |
pharmgkb | rs786204165 |
gwascentral | rs786204165 |
openSNP | rs786204165 |
23andMe | rs786204165 |
SNPshot | rs786204165 |
SNPdbe | rs786204165 |
MSV3d | rs786204165 |
GWAS Ctlg | rs786204165 |
Status | Merged into rs587781276 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | |
Alt | |
Reference | Rs786204165(TG;TG) |
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.68857429_68857430delTG |
CLNSRC | |
CLNACC | RCV000128928.2, RCV000168178.1, |