rs1057517248
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs1057517248(-;-) |
Make rs1057517248(-;A) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 11 |
Position | 108256215 |
Gene | ATM |
is a | snp |
is | mentioned by |
dbSNP | rs1057517248 |
dbSNP (classic) | rs1057517248 |
ClinGen | rs1057517248 |
ebi | rs1057517248 |
HLI | rs1057517248 |
Exac | rs1057517248 |
Gnomad | rs1057517248 |
Varsome | rs1057517248 |
LitVar | rs1057517248 |
Map | rs1057517248 |
PheGenI | rs1057517248 |
Biobank | rs1057517248 |
1000 genomes | rs1057517248 |
hgdp | rs1057517248 |
ensembl | rs1057517248 |
geneview | rs1057517248 |
scholar | rs1057517248 |
rs1057517248 | |
pharmgkb | rs1057517248 |
gwascentral | rs1057517248 |
openSNP | rs1057517248 |
23andMe | rs1057517248 |
SNPshot | rs1057517248 |
SNPdbe | rs1057517248 |
MSV3d | rs1057517248 |
GWAS Ctlg | rs1057517248 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1057517248(-;-) |
Alt | rs1057517248(-;-) |
Reference | Rs1057517248(A;A) |
Significance | Probable-Pathogenic |
Disease | Ataxia-telangiectasia syndrome |
Variation | info |
Gene | ATM |
CLNDBN | Ataxia-telangiectasia syndrome |
Reversed | 0 |
HGVS | NC_000011.9:g.108126942delA |
CLNSRC | |
CLNACC | RCV000412308.1, |