rs863224508
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs863224508(-;-) |
Make rs863224508(-;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 94464195 |
Gene | MRE11A |
is a | snp |
is | mentioned by |
dbSNP | rs863224508 |
dbSNP (classic) | rs863224508 |
ClinGen | rs863224508 |
ebi | rs863224508 |
HLI | rs863224508 |
Exac | rs863224508 |
Gnomad | rs863224508 |
Varsome | rs863224508 |
LitVar | rs863224508 |
Map | rs863224508 |
PheGenI | rs863224508 |
Biobank | rs863224508 |
1000 genomes | rs863224508 |
hgdp | rs863224508 |
ensembl | rs863224508 |
geneview | rs863224508 |
scholar | rs863224508 |
rs863224508 | |
pharmgkb | rs863224508 |
gwascentral | rs863224508 |
openSNP | rs863224508 |
23andMe | rs863224508 |
SNPshot | rs863224508 |
SNPdbe | rs863224508 |
MSV3d | rs863224508 |
GWAS Ctlg | rs863224508 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs863224508(-;-) |
Alt | rs863224508(-;-) |
Reference | Rs863224508(T;T) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | MRE11A |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000011.9:g.94197361delA |
CLNSRC | |
CLNACC | RCV000197350.1, |