rs886037822
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs886037822(-;-) |
Make rs886037822(-;C) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 16 |
Position | 68813395 |
Gene | CDH1 |
is a | snp |
is | mentioned by |
dbSNP | rs886037822 |
dbSNP (classic) | rs886037822 |
ClinGen | rs886037822 |
ebi | rs886037822 |
HLI | rs886037822 |
Exac | rs886037822 |
Gnomad | rs886037822 |
Varsome | rs886037822 |
LitVar | rs886037822 |
Map | rs886037822 |
PheGenI | rs886037822 |
Biobank | rs886037822 |
1000 genomes | rs886037822 |
hgdp | rs886037822 |
ensembl | rs886037822 |
geneview | rs886037822 |
scholar | rs886037822 |
rs886037822 | |
pharmgkb | rs886037822 |
gwascentral | rs886037822 |
openSNP | rs886037822 |
23andMe | rs886037822 |
SNPshot | rs886037822 |
SNPdbe | rs886037822 |
MSV3d | rs886037822 |
GWAS Ctlg | rs886037822 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs886037822(-;-) |
Alt | rs886037822(-;-) |
Reference | Rs886037822(C;C) |
Significance | Pathogenic |
Disease | Hereditary diffuse gastric cancer |
Variation | info |
Gene | CDH1 |
CLNDBN | Hereditary diffuse gastric cancer |
Reversed | 0 |
HGVS | NC_000016.9:g.68847298delC |
CLNSRC | |
CLNACC | RCV000240878.1, |