rs765059994
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs765059994(C;G) |
Make rs765059994(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 14 |
Position | 95099779 |
Gene | DICER1 |
is a | snp |
is | mentioned by |
dbSNP | rs765059994 |
dbSNP (classic) | rs765059994 |
ClinGen | rs765059994 |
ebi | rs765059994 |
HLI | rs765059994 |
Exac | rs765059994 |
Gnomad | rs765059994 |
Varsome | rs765059994 |
LitVar | rs765059994 |
Map | rs765059994 |
PheGenI | rs765059994 |
Biobank | rs765059994 |
1000 genomes | rs765059994 |
hgdp | rs765059994 |
ensembl | rs765059994 |
geneview | rs765059994 |
scholar | rs765059994 |
rs765059994 | |
pharmgkb | rs765059994 |
gwascentral | rs765059994 |
openSNP | rs765059994 |
23andMe | rs765059994 |
SNPshot | rs765059994 |
SNPdbe | rs765059994 |
MSV3d | rs765059994 |
GWAS Ctlg | rs765059994 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs765059994(G;G) |
Alt | rs765059994(G;G) |
Reference | Rs765059994(C;C) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | DICER1 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000014.8:g.95566116C>A |
CLNSRC | |
CLNACC | RCV000493925.1, |