rs1018140779
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 11 |
Position | 108329097 |
Gene | ATM, C11orf65 |
is a | snp |
is | mentioned by |
dbSNP | rs1018140779 |
dbSNP (classic) | rs1018140779 |
ClinGen | rs1018140779 |
ebi | rs1018140779 |
HLI | rs1018140779 |
Exac | rs1018140779 |
Gnomad | rs1018140779 |
Varsome | rs1018140779 |
LitVar | rs1018140779 |
Map | rs1018140779 |
PheGenI | rs1018140779 |
Biobank | rs1018140779 |
1000 genomes | rs1018140779 |
hgdp | rs1018140779 |
ensembl | rs1018140779 |
geneview | rs1018140779 |
scholar | rs1018140779 |
rs1018140779 | |
pharmgkb | rs1018140779 |
gwascentral | rs1018140779 |
openSNP | rs1018140779 |
23andMe | rs1018140779 |
SNPshot | rs1018140779 |
SNPdbe | rs1018140779 |
MSV3d | rs1018140779 |
GWAS Ctlg | rs1018140779 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1018140779(T;T) |
Alt | rs1018140779(T;T) |
Reference | Rs1018140779(C;C) |
Significance | Probable-Pathogenic |
Disease | Ataxia-telangiectasia syndrome not specified |
Variation | info |
Gene | |
CLNDBN | Ataxia-telangiectasia syndrome not specified |
Reversed | 0 |
HGVS | NC_000011.9:g.108199824C>G; NC_000011.9:g.108199824C>T |
CLNSRC | |
CLNACC | RCV000411247.1, RCV000436625.1, |