rs780001540
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs780001540(A;A) |
Make rs780001540(A;G) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 11 |
Position | 94459461 |
Gene | MRE11A |
is a | snp |
is | mentioned by |
dbSNP | rs780001540 |
dbSNP (classic) | rs780001540 |
ClinGen | rs780001540 |
ebi | rs780001540 |
HLI | rs780001540 |
Exac | rs780001540 |
Gnomad | rs780001540 |
Varsome | rs780001540 |
LitVar | rs780001540 |
Map | rs780001540 |
PheGenI | rs780001540 |
Biobank | rs780001540 |
1000 genomes | rs780001540 |
hgdp | rs780001540 |
ensembl | rs780001540 |
geneview | rs780001540 |
scholar | rs780001540 |
rs780001540 | |
pharmgkb | rs780001540 |
gwascentral | rs780001540 |
openSNP | rs780001540 |
23andMe | rs780001540 |
SNPshot | rs780001540 |
SNPdbe | rs780001540 |
MSV3d | rs780001540 |
GWAS Ctlg | rs780001540 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs780001540(A;A) |
Alt | rs780001540(A;A) |
Reference | Rs780001540(G;G) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | MRE11A |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000011.9:g.94192627G>A |
CLNSRC | |
CLNACC | RCV000216978.1, |