rs786203807
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;C) | 6 | Breast cancer associated mutation |
(C;C) | 0 | common in clinvar |
Make rs786203807(-;-) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 108256219 |
Gene | ATM |
is a | snp |
is | mentioned by |
dbSNP | rs786203807 |
dbSNP (classic) | rs786203807 |
ClinGen | rs786203807 |
ebi | rs786203807 |
HLI | rs786203807 |
Exac | rs786203807 |
Gnomad | rs786203807 |
Varsome | rs786203807 |
LitVar | rs786203807 |
Map | rs786203807 |
PheGenI | rs786203807 |
Biobank | rs786203807 |
1000 genomes | rs786203807 |
hgdp | rs786203807 |
ensembl | rs786203807 |
geneview | rs786203807 |
scholar | rs786203807 |
rs786203807 | |
pharmgkb | rs786203807 |
gwascentral | rs786203807 |
openSNP | rs786203807 |
23andMe | rs786203807 |
SNPshot | rs786203807 |
SNPdbe | rs786203807 |
MSV3d | rs786203807 |
GWAS Ctlg | rs786203807 |
Max Magnitude | 6 |
ClinVar | |
---|---|
Risk | rs786203807(-;-) |
Alt | rs786203807(-;-) |
Reference | Rs786203807(C;C) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | ATM |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000011.9:g.108126946delC |
CLNSRC | |
CLNACC | RCV000167269.1, |