rs745677716
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs745677716(A;G) |
Make rs745677716(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 11 |
Position | 94445808 |
Gene | MRE11A |
is a | snp |
is | mentioned by |
dbSNP | rs745677716 |
dbSNP (classic) | rs745677716 |
ClinGen | rs745677716 |
ebi | rs745677716 |
HLI | rs745677716 |
Exac | rs745677716 |
Gnomad | rs745677716 |
Varsome | rs745677716 |
LitVar | rs745677716 |
Map | rs745677716 |
PheGenI | rs745677716 |
Biobank | rs745677716 |
1000 genomes | rs745677716 |
hgdp | rs745677716 |
ensembl | rs745677716 |
geneview | rs745677716 |
scholar | rs745677716 |
rs745677716 | |
pharmgkb | rs745677716 |
gwascentral | rs745677716 |
openSNP | rs745677716 |
23andMe | rs745677716 |
SNPshot | rs745677716 |
SNPdbe | rs745677716 |
MSV3d | rs745677716 |
GWAS Ctlg | rs745677716 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs745677716(G;G) |
Alt | rs745677716(G;G) |
Reference | Rs745677716(A;A) |
Significance | Probable-Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | MRE11A |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000011.9:g.94178974A>G |
CLNSRC | |
CLNACC | RCV000166874.2, |