rs202206540
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs202206540(A;A) |
Make rs202206540(A;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 11 |
Position | 108316069 |
Gene | ATM, C11orf65 |
is a | snp |
is | mentioned by |
dbSNP | rs202206540 |
dbSNP (classic) | rs202206540 |
ClinGen | rs202206540 |
ebi | rs202206540 |
HLI | rs202206540 |
Exac | rs202206540 |
Gnomad | rs202206540 |
Varsome | rs202206540 |
LitVar | rs202206540 |
Map | rs202206540 |
PheGenI | rs202206540 |
Biobank | rs202206540 |
1000 genomes | rs202206540 |
hgdp | rs202206540 |
ensembl | rs202206540 |
geneview | rs202206540 |
scholar | rs202206540 |
rs202206540 | |
pharmgkb | rs202206540 |
gwascentral | rs202206540 |
openSNP | rs202206540 |
23andMe | rs202206540 |
SNPshot | rs202206540 |
SNPdbe | rs202206540 |
MSV3d | rs202206540 |
GWAS Ctlg | rs202206540 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs202206540(A;A) |
Alt | rs202206540(A;A) |
Reference | Rs202206540(G;G) |
Significance | Other |
Disease | Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not specified |
Variation | info |
Gene | C11orf65 ATM |
CLNDBN | Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not specified |
Reversed | 0 |
HGVS | NC_000011.9:g.108186796G>A |
CLNSRC | |
CLNACC | RCV000159743.5, RCV000167963.3, RCV000212039.1, |