rs3092857
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in complete genomics |
Make rs3092857(A;G) |
Make rs3092857(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 108272572 |
Gene | ATM |
is a | snp |
is | mentioned by |
dbSNP | rs3092857 |
dbSNP (classic) | rs3092857 |
ClinGen | rs3092857 |
ebi | rs3092857 |
HLI | rs3092857 |
Exac | rs3092857 |
Gnomad | rs3092857 |
Varsome | rs3092857 |
LitVar | rs3092857 |
Map | rs3092857 |
PheGenI | rs3092857 |
Biobank | rs3092857 |
1000 genomes | rs3092857 |
hgdp | rs3092857 |
ensembl | rs3092857 |
geneview | rs3092857 |
scholar | rs3092857 |
rs3092857 | |
pharmgkb | rs3092857 |
gwascentral | rs3092857 |
openSNP | rs3092857 |
23andMe | rs3092857 |
SNPshot | rs3092857 |
SNPdbe | rs3092857 |
MSV3d | rs3092857 |
GWAS Ctlg | rs3092857 |
GMAF | 0.01102 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
NOTE: the OMIM entry cited below refers to a somatic mutation, not a germline SNP
ClinVar | |
---|---|
Risk | rs3092857(G;G) |
Alt | rs3092857(G;G) |
Reference | Rs3092857(A;A) |
Significance | Other |
Disease | B-cell non-Hodgkin lymphoma not specified Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided |
Variation | info |
Gene | ATM |
CLNDBN | B-cell non-Hodgkin lymphoma not specified Hereditary cancer-predisposing syndrome Ataxia-telangiectasia syndrome not provided |
Reversed | 0 |
HGVS | NC_000011.9:g.108143299A>G |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000003166.4, RCV000116423.4, RCV000123734.4, RCV000203947.3, RCV000224788.1, |