rs1801026
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs1801026(C;T) |
Make rs1801026(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 68833553 |
Gene | CDH1 |
is a | snp |
is | mentioned by |
dbSNP | rs1801026 |
dbSNP (classic) | rs1801026 |
ClinGen | rs1801026 |
ebi | rs1801026 |
HLI | rs1801026 |
Exac | rs1801026 |
Gnomad | rs1801026 |
Varsome | rs1801026 |
LitVar | rs1801026 |
Map | rs1801026 |
PheGenI | rs1801026 |
Biobank | rs1801026 |
1000 genomes | rs1801026 |
hgdp | rs1801026 |
ensembl | rs1801026 |
geneview | rs1801026 |
scholar | rs1801026 |
rs1801026 | |
pharmgkb | rs1801026 |
gwascentral | rs1801026 |
openSNP | rs1801026 |
23andMe | rs1801026 |
SNPshot | rs1801026 |
SNPdbe | rs1801026 |
MSV3d | rs1801026 |
GWAS Ctlg | rs1801026 |
Max Magnitude | 0 |
[PMID 25150394] Genetic variation of the E-cadherin gene is associated with primary infertility in patients with ovarian endometriosis
[PMID 27852262] E-cadherin genetic variants predict survival outcome in breast cancer patients.
ClinVar | |
---|---|
Risk | rs1801026(A;A) rs1801026(G;G) rs1801026(T;T) |
Alt | rs1801026(A;A) rs1801026(G;G) rs1801026(T;T) |
Reference | Rs1801026(C;C) |
Significance | Non-pathogenic |
Disease | Hereditary diffuse gastric cancer |
Variation | info |
Gene | CDH1 |
CLNDBN | Hereditary diffuse gastric cancer |
Reversed | 0 |
HGVS | NC_000016.9:g.68867456C>T |
CLNSRC | |
CLNACC | RCV000325599.1, |