rs786202764
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs786202764(-;C) |
Make rs786202764(C;C) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 94464202 |
Gene | MRE11A |
is a | snp |
is | mentioned by |
dbSNP | rs786202764 |
dbSNP (classic) | rs786202764 |
ClinGen | rs786202764 |
ebi | rs786202764 |
HLI | rs786202764 |
Exac | rs786202764 |
Gnomad | rs786202764 |
Varsome | rs786202764 |
LitVar | rs786202764 |
Map | rs786202764 |
PheGenI | rs786202764 |
Biobank | rs786202764 |
1000 genomes | rs786202764 |
hgdp | rs786202764 |
ensembl | rs786202764 |
geneview | rs786202764 |
scholar | rs786202764 |
rs786202764 | |
pharmgkb | rs786202764 |
gwascentral | rs786202764 |
openSNP | rs786202764 |
23andMe | rs786202764 |
SNPshot | rs786202764 |
SNPdbe | rs786202764 |
MSV3d | rs786202764 |
GWAS Ctlg | rs786202764 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786202764(C;C) |
Alt | rs786202764(C;C) |
Reference | Rs786202764(-;-) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | MRE11A |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000011.9:g.94197369dupG |
CLNSRC | |
CLNACC | RCV000165739.2, |