rs1060501695
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs1060501695(C;G) |
Make rs1060501695(G;G) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 11 |
Position | 108335098 |
Gene | ATM, C11orf65 |
is a | snp |
is | mentioned by |
dbSNP | rs1060501695 |
dbSNP (classic) | rs1060501695 |
ClinGen | rs1060501695 |
ebi | rs1060501695 |
HLI | rs1060501695 |
Exac | rs1060501695 |
Gnomad | rs1060501695 |
Varsome | rs1060501695 |
LitVar | rs1060501695 |
Map | rs1060501695 |
PheGenI | rs1060501695 |
Biobank | rs1060501695 |
1000 genomes | rs1060501695 |
hgdp | rs1060501695 |
ensembl | rs1060501695 |
geneview | rs1060501695 |
scholar | rs1060501695 |
rs1060501695 | |
pharmgkb | rs1060501695 |
gwascentral | rs1060501695 |
openSNP | rs1060501695 |
23andMe | rs1060501695 |
SNPshot | rs1060501695 |
SNPdbe | rs1060501695 |
MSV3d | rs1060501695 |
GWAS Ctlg | rs1060501695 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1060501695(G;G) rs1060501695(T;T) |
Alt | rs1060501695(G;G) rs1060501695(T;T) |
Reference | Rs1060501695(C;C) |
Significance | Pathogenic |
Disease | Ataxia-telangiectasia syndrome not provided |
Variation | info |
Gene | C11orf65 ATM |
CLNDBN | Ataxia-telangiectasia syndrome not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.108205825C>G; NC_000011.9:g.108205825C>T |
CLNSRC | |
CLNACC | RCV000471423.1, RCV000480590.1, |