rs587780119
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs587780119(A;T) |
Make rs587780119(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 16 |
Position | 68829701 |
Gene | CDH1 |
is a | snp |
is | mentioned by |
dbSNP | rs587780119 |
dbSNP (classic) | rs587780119 |
ClinGen | rs587780119 |
ebi | rs587780119 |
HLI | rs587780119 |
Exac | rs587780119 |
Gnomad | rs587780119 |
Varsome | rs587780119 |
LitVar | rs587780119 |
Map | rs587780119 |
PheGenI | rs587780119 |
Biobank | rs587780119 |
1000 genomes | rs587780119 |
hgdp | rs587780119 |
ensembl | rs587780119 |
geneview | rs587780119 |
scholar | rs587780119 |
rs587780119 | |
pharmgkb | rs587780119 |
gwascentral | rs587780119 |
openSNP | rs587780119 |
23andMe | rs587780119 |
SNPshot | rs587780119 |
SNPdbe | rs587780119 |
MSV3d | rs587780119 |
GWAS Ctlg | rs587780119 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587780119(G;G) rs587780119(T;T) |
Alt | rs587780119(G;G) rs587780119(T;T) |
Reference | Rs587780119(A;A) |
Significance | Probable-non-pathogenic |
Disease | Hereditary cancer-predisposing syndrome not specified Hereditary diffuse gastric cancer |
Variation | info |
Gene | CDH1 |
CLNDBN | Hereditary cancer-predisposing syndrome not specified Hereditary diffuse gastric cancer |
Reversed | 0 |
HGVS | NC_000016.9:g.68863604A>G; NC_000016.9:g.68863604A>T |
CLNSRC | |
CLNACC | RCV000163882.1, RCV000445087.1, RCV000475098.1, RCV000115852.6, RCV000225693.2, RCV000234640.2, |