rs3092844
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs3092844(C;T) |
Make rs3092844(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 108368580 |
Gene | ATM, C11orf65 |
is a | snp |
is | mentioned by |
dbSNP | rs3092844 |
dbSNP (classic) | rs3092844 |
ClinGen | rs3092844 |
ebi | rs3092844 |
HLI | rs3092844 |
Exac | rs3092844 |
Gnomad | rs3092844 |
Varsome | rs3092844 |
LitVar | rs3092844 |
Map | rs3092844 |
PheGenI | rs3092844 |
Biobank | rs3092844 |
1000 genomes | rs3092844 |
hgdp | rs3092844 |
ensembl | rs3092844 |
geneview | rs3092844 |
scholar | rs3092844 |
rs3092844 | |
pharmgkb | rs3092844 |
gwascentral | rs3092844 |
openSNP | rs3092844 |
23andMe | rs3092844 |
SNPshot | rs3092844 |
SNPdbe | rs3092844 |
MSV3d | rs3092844 |
GWAS Ctlg | rs3092844 |
GMAF | 0.04591 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 22529920] Computational Refinement of Functional Single Nucleotide Polymorphisms Associated with ATM Gene
ClinVar | |
---|---|
Risk | rs3092844(A;A) rs3092844(T;T) |
Alt | rs3092844(A;A) rs3092844(T;T) |
Reference | Rs3092844(C;C) |
Significance | Probable-non-pathogenic |
Disease | Ataxia-telangiectasia syndrome |
Variation | info |
Gene | C11orf65 ATM |
CLNDBN | Ataxia-telangiectasia syndrome |
Reversed | 0 |
HGVS | NC_000011.9:g.108239307C>T |
CLNSRC | |
CLNACC | RCV000343133.1, |