rs730881303
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs730881303(-;-) |
Make rs730881303(-;A) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 11 |
Position | 108229229 |
Gene | ATM |
is a | snp |
is | mentioned by |
dbSNP | rs730881303 |
dbSNP (classic) | rs730881303 |
ClinGen | rs730881303 |
ebi | rs730881303 |
HLI | rs730881303 |
Exac | rs730881303 |
Gnomad | rs730881303 |
Varsome | rs730881303 |
LitVar | rs730881303 |
Map | rs730881303 |
PheGenI | rs730881303 |
Biobank | rs730881303 |
1000 genomes | rs730881303 |
hgdp | rs730881303 |
ensembl | rs730881303 |
geneview | rs730881303 |
scholar | rs730881303 |
rs730881303 | |
pharmgkb | rs730881303 |
gwascentral | rs730881303 |
openSNP | rs730881303 |
23andMe | rs730881303 |
SNPshot | rs730881303 |
SNPdbe | rs730881303 |
MSV3d | rs730881303 |
GWAS Ctlg | rs730881303 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs730881303(-;-) |
Alt | rs730881303(-;-) |
Reference | Rs730881303(A;A) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | ATM |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.108099956delA |
CLNSRC | |
CLNACC | RCV000159632.2, |