rs772926890
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs772926890(G;T) |
Make rs772926890(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 108251073 |
Gene | ATM |
is a | snp |
is | mentioned by |
dbSNP | rs772926890 |
dbSNP (classic) | rs772926890 |
ClinGen | rs772926890 |
ebi | rs772926890 |
HLI | rs772926890 |
Exac | rs772926890 |
Gnomad | rs772926890 |
Varsome | rs772926890 |
LitVar | rs772926890 |
Map | rs772926890 |
PheGenI | rs772926890 |
Biobank | rs772926890 |
1000 genomes | rs772926890 |
hgdp | rs772926890 |
ensembl | rs772926890 |
geneview | rs772926890 |
scholar | rs772926890 |
rs772926890 | |
pharmgkb | rs772926890 |
gwascentral | rs772926890 |
openSNP | rs772926890 |
23andMe | rs772926890 |
SNPshot | rs772926890 |
SNPdbe | rs772926890 |
MSV3d | rs772926890 |
GWAS Ctlg | rs772926890 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs772926890(T;T) |
Alt | rs772926890(T;T) |
Reference | Rs772926890(G;G) |
Significance | Other |
Disease | Ataxia-telangiectasia syndrome not provided |
Variation | info |
Gene | ATM |
CLNDBN | Ataxia-telangiectasia syndrome not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.108121800G>T |
CLNSRC | |
CLNACC | RCV000203930.1, RCV000235749.1, |