rs587782895
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AA;AA) | 0 | common in clinvar |
Make rs587782895(-;-) |
Make rs587782895(-;AA) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 5 |
Position | 132604020 |
Gene | RAD50 |
is a | snp |
is | mentioned by |
dbSNP | rs587782895 |
dbSNP (classic) | rs587782895 |
ClinGen | rs587782895 |
ebi | rs587782895 |
HLI | rs587782895 |
Exac | rs587782895 |
Gnomad | rs587782895 |
Varsome | rs587782895 |
LitVar | rs587782895 |
Map | rs587782895 |
PheGenI | rs587782895 |
Biobank | rs587782895 |
1000 genomes | rs587782895 |
hgdp | rs587782895 |
ensembl | rs587782895 |
geneview | rs587782895 |
scholar | rs587782895 |
rs587782895 | |
pharmgkb | rs587782895 |
gwascentral | rs587782895 |
openSNP | rs587782895 |
23andMe | rs587782895 |
SNPshot | rs587782895 |
SNPdbe | rs587782895 |
MSV3d | rs587782895 |
GWAS Ctlg | rs587782895 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587782895(-;-) |
Alt | rs587782895(-;-) |
Reference | Rs587782895(AA;AA) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | RAD50 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.131939712_131939713delAA |
CLNSRC | |
CLNACC | RCV000132534.3, |