rs786203931
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs786203931(-;C) |
Make rs786203931(C;C) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 11 |
Position | 94471679 |
Gene | MRE11A |
is a | snp |
is | mentioned by |
dbSNP | rs786203931 |
dbSNP (classic) | rs786203931 |
ClinGen | rs786203931 |
ebi | rs786203931 |
HLI | rs786203931 |
Exac | rs786203931 |
Gnomad | rs786203931 |
Varsome | rs786203931 |
LitVar | rs786203931 |
Map | rs786203931 |
PheGenI | rs786203931 |
Biobank | rs786203931 |
1000 genomes | rs786203931 |
hgdp | rs786203931 |
ensembl | rs786203931 |
geneview | rs786203931 |
scholar | rs786203931 |
rs786203931 | |
pharmgkb | rs786203931 |
gwascentral | rs786203931 |
openSNP | rs786203931 |
23andMe | rs786203931 |
SNPshot | rs786203931 |
SNPdbe | rs786203931 |
MSV3d | rs786203931 |
GWAS Ctlg | rs786203931 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786203931(C;C) |
Alt | rs786203931(C;C) |
Reference | Rs786203931(-;-) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | MRE11A |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 1 |
HGVS | NC_000011.9:g.94204846dupG |
CLNSRC | |
CLNACC | RCV000167449.1, |