rs587782030
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs587782030(C;T) |
Make rs587782030(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 11 |
Position | 94478771 |
Gene | MRE11A |
is a | snp |
is | mentioned by |
dbSNP | rs587782030 |
dbSNP (classic) | rs587782030 |
ClinGen | rs587782030 |
ebi | rs587782030 |
HLI | rs587782030 |
Exac | rs587782030 |
Gnomad | rs587782030 |
Varsome | rs587782030 |
LitVar | rs587782030 |
Map | rs587782030 |
PheGenI | rs587782030 |
Biobank | rs587782030 |
1000 genomes | rs587782030 |
hgdp | rs587782030 |
ensembl | rs587782030 |
geneview | rs587782030 |
scholar | rs587782030 |
rs587782030 | |
pharmgkb | rs587782030 |
gwascentral | rs587782030 |
openSNP | rs587782030 |
23andMe | rs587782030 |
SNPshot | rs587782030 |
SNPdbe | rs587782030 |
MSV3d | rs587782030 |
GWAS Ctlg | rs587782030 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587782030(A;A) rs587782030(T;T) |
Alt | rs587782030(A;A) rs587782030(T;T) |
Reference | Rs587782030(C;C) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome Ataxia-telangiectasia-like disorder 1 |
Variation | info |
Gene | MRE11A |
CLNDBN | Hereditary cancer-predisposing syndrome Ataxia-telangiectasia-like disorder 1 |
Reversed | 1 |
HGVS | NC_000011.9:g.94211937G>A; NC_000011.9:g.94211937G>T |
CLNSRC | |
CLNACC | RCV000130478.2, RCV000308108.1, |