rs137852761
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs137852761(C;T) |
Make rs137852761(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 94447288 |
Gene | MRE11A |
is a | snp |
is | mentioned by |
dbSNP | rs137852761 |
dbSNP (classic) | rs137852761 |
ClinGen | rs137852761 |
ebi | rs137852761 |
HLI | rs137852761 |
Exac | rs137852761 |
Gnomad | rs137852761 |
Varsome | rs137852761 |
LitVar | rs137852761 |
Map | rs137852761 |
PheGenI | rs137852761 |
Biobank | rs137852761 |
1000 genomes | rs137852761 |
hgdp | rs137852761 |
ensembl | rs137852761 |
geneview | rs137852761 |
scholar | rs137852761 |
rs137852761 | |
pharmgkb | rs137852761 |
gwascentral | rs137852761 |
openSNP | rs137852761 |
23andMe | rs137852761 |
SNPshot | rs137852761 |
SNPdbe | rs137852761 |
MSV3d | rs137852761 |
GWAS Ctlg | rs137852761 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs137852761(T;T) |
Alt | rs137852761(T;T) |
Reference | Rs137852761(C;C) |
Significance | Pathogenic |
Disease | Ataxia-telangiectasia-like disorder 1 Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | MRE11A |
CLNDBN | Ataxia-telangiectasia-like disorder 1 Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000011.9:g.94180454G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000009329.3, RCV000130661.3, |