rs776912688
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs776912688(A;A) |
Make rs776912688(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 94471613 |
Gene | MRE11, MRE11A |
is a | snp |
is | mentioned by |
dbSNP | rs776912688 |
dbSNP (classic) | rs776912688 |
ClinGen | rs776912688 |
ebi | rs776912688 |
HLI | rs776912688 |
Exac | rs776912688 |
Gnomad | rs776912688 |
Varsome | rs776912688 |
LitVar | rs776912688 |
Map | rs776912688 |
PheGenI | rs776912688 |
Biobank | rs776912688 |
1000 genomes | rs776912688 |
hgdp | rs776912688 |
ensembl | rs776912688 |
geneview | rs776912688 |
scholar | rs776912688 |
rs776912688 | |
pharmgkb | rs776912688 |
gwascentral | rs776912688 |
openSNP | rs776912688 |
23andMe | rs776912688 |
SNPshot | rs776912688 |
SNPdbe | rs776912688 |
MSV3d | rs776912688 |
GWAS Ctlg | rs776912688 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs776912688(A;A) rs776912688(C;C) |
Alt | rs776912688(A;A) rs776912688(C;C) |
Reference | Rs776912688(G;G) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | MRE11 MRE11A |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000011.9:g.94204779G>C |
CLNSRC | |
CLNACC | RCV000219565.1, |