rs587781822
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs587781822(A;G) |
Make rs587781822(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 11 |
Position | 94435901 |
Gene | MRE11A |
is a | snp |
is | mentioned by |
dbSNP | rs587781822 |
dbSNP (classic) | rs587781822 |
ClinGen | rs587781822 |
ebi | rs587781822 |
HLI | rs587781822 |
Exac | rs587781822 |
Gnomad | rs587781822 |
Varsome | rs587781822 |
LitVar | rs587781822 |
Map | rs587781822 |
PheGenI | rs587781822 |
Biobank | rs587781822 |
1000 genomes | rs587781822 |
hgdp | rs587781822 |
ensembl | rs587781822 |
geneview | rs587781822 |
scholar | rs587781822 |
rs587781822 | |
pharmgkb | rs587781822 |
gwascentral | rs587781822 |
openSNP | rs587781822 |
23andMe | rs587781822 |
SNPshot | rs587781822 |
SNPdbe | rs587781822 |
MSV3d | rs587781822 |
GWAS Ctlg | rs587781822 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587781822(G;G) |
Alt | rs587781822(G;G) |
Reference | Rs587781822(A;A) |
Significance | Probable-Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | MRE11A |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000011.9:g.94169067T>C |
CLNSRC | |
CLNACC | RCV000130102.4, |