rs587779851
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs587779851(CCT;CCT) |
Make rs587779851(CCT;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 11 |
Position | 108310188 |
Gene | ATM, C11orf65 |
is a | snp |
is | mentioned by |
dbSNP | rs587779851 |
dbSNP (classic) | rs587779851 |
ClinGen | rs587779851 |
ebi | rs587779851 |
HLI | rs587779851 |
Exac | rs587779851 |
Gnomad | rs587779851 |
Varsome | rs587779851 |
LitVar | rs587779851 |
Map | rs587779851 |
PheGenI | rs587779851 |
Biobank | rs587779851 |
1000 genomes | rs587779851 |
hgdp | rs587779851 |
ensembl | rs587779851 |
geneview | rs587779851 |
scholar | rs587779851 |
rs587779851 | |
pharmgkb | rs587779851 |
gwascentral | rs587779851 |
openSNP | rs587779851 |
23andMe | rs587779851 |
SNPshot | rs587779851 |
SNPdbe | rs587779851 |
MSV3d | rs587779851 |
GWAS Ctlg | rs587779851 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587779851(CCT;CCT) |
Alt | rs587779851(CCT;CCT) |
Reference | Rs587779851(G;G) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome not provided Ataxia-telangiectasia syndrome |
Variation | info |
Gene | C11orf65 ATM |
CLNDBN | Hereditary cancer-predisposing syndrome not provided Ataxia-telangiectasia syndrome |
Reversed | 0 |
HGVS | NC_000011.9:g.108180915delGinsCCT |
CLNSRC | |
CLNACC | RCV000115216.7, RCV000235106.2, RCV000409117.1, |