rs587781658
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(CT;CT) | 0 | common in clinvar |
Make rs587781658(-;-) |
Make rs587781658(-;CT) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 11 |
Position | 108257514 |
Gene | ATM |
is a | snp |
is | mentioned by |
dbSNP | rs587781658 |
dbSNP (classic) | rs587781658 |
ClinGen | rs587781658 |
ebi | rs587781658 |
HLI | rs587781658 |
Exac | rs587781658 |
Gnomad | rs587781658 |
Varsome | rs587781658 |
LitVar | rs587781658 |
Map | rs587781658 |
PheGenI | rs587781658 |
Biobank | rs587781658 |
1000 genomes | rs587781658 |
hgdp | rs587781658 |
ensembl | rs587781658 |
geneview | rs587781658 |
scholar | rs587781658 |
rs587781658 | |
pharmgkb | rs587781658 |
gwascentral | rs587781658 |
openSNP | rs587781658 |
23andMe | rs587781658 |
SNPshot | rs587781658 |
SNPdbe | rs587781658 |
MSV3d | rs587781658 |
GWAS Ctlg | rs587781658 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587781658(-;-) |
Alt | rs587781658(-;-) |
Reference | Rs587781658(CT;CT) |
Significance | Other |
Disease | Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided |
Variation | info |
Gene | ATM |
CLNDBN | Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.108128241_108128242delCT |
CLNSRC | |
CLNACC | RCV000129801.4, RCV000233154.2, RCV000480339.1, |