rs747832587
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs747832587(-;-) |
Make rs747832587(-;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 94459467 |
Gene | MRE11A |
is a | snp |
is | mentioned by |
dbSNP | rs747832587 |
dbSNP (classic) | rs747832587 |
ClinGen | rs747832587 |
ebi | rs747832587 |
HLI | rs747832587 |
Exac | rs747832587 |
Gnomad | rs747832587 |
Varsome | rs747832587 |
LitVar | rs747832587 |
Map | rs747832587 |
PheGenI | rs747832587 |
Biobank | rs747832587 |
1000 genomes | rs747832587 |
hgdp | rs747832587 |
ensembl | rs747832587 |
geneview | rs747832587 |
scholar | rs747832587 |
rs747832587 | |
pharmgkb | rs747832587 |
gwascentral | rs747832587 |
openSNP | rs747832587 |
23andMe | rs747832587 |
SNPshot | rs747832587 |
SNPdbe | rs747832587 |
MSV3d | rs747832587 |
GWAS Ctlg | rs747832587 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs747832587(-;-) |
Alt | rs747832587(-;-) |
Reference | Rs747832587(T;T) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | MRE11A |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000011.9:g.94192633delT |
CLNSRC | |
CLNACC | RCV000199221.1, |