rs876658865
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CCC;CCC) | 0 | common in clinvar |
Chromosome | 16 |
Position | 68738372 |
Gene | CDH1 |
is a | snp |
is | mentioned by |
dbSNP | rs876658865 |
dbSNP (classic) | rs876658865 |
ClinGen | rs876658865 |
ebi | rs876658865 |
HLI | rs876658865 |
Exac | rs876658865 |
Gnomad | rs876658865 |
Varsome | rs876658865 |
LitVar | rs876658865 |
Map | rs876658865 |
PheGenI | rs876658865 |
Biobank | rs876658865 |
1000 genomes | rs876658865 |
hgdp | rs876658865 |
ensembl | rs876658865 |
geneview | rs876658865 |
scholar | rs876658865 |
rs876658865 | |
pharmgkb | rs876658865 |
gwascentral | rs876658865 |
openSNP | rs876658865 |
23andMe | rs876658865 |
SNPshot | rs876658865 |
SNPdbe | rs876658865 |
MSV3d | rs876658865 |
GWAS Ctlg | rs876658865 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs876658865(T;T) |
Alt | rs876658865(T;T) |
Reference | Rs876658865(CCC;CCC) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | CDH1 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000016.9:g.68772275_68772277delCCCinsT |
CLNSRC | |
CLNACC | RCV000215517.1, |