rs587780147
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs587780147(-;GATAAGA) |
Make rs587780147(GATAAGA;GATAAGA) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 5 |
Position | 132589691 |
Gene | RAD50 |
is a | snp |
is | mentioned by |
dbSNP | rs587780147 |
dbSNP (classic) | rs587780147 |
ClinGen | rs587780147 |
ebi | rs587780147 |
HLI | rs587780147 |
Exac | rs587780147 |
Gnomad | rs587780147 |
Varsome | rs587780147 |
LitVar | rs587780147 |
Map | rs587780147 |
PheGenI | rs587780147 |
Biobank | rs587780147 |
1000 genomes | rs587780147 |
hgdp | rs587780147 |
ensembl | rs587780147 |
geneview | rs587780147 |
scholar | rs587780147 |
rs587780147 | |
pharmgkb | rs587780147 |
gwascentral | rs587780147 |
openSNP | rs587780147 |
23andMe | rs587780147 |
SNPshot | rs587780147 |
SNPdbe | rs587780147 |
MSV3d | rs587780147 |
GWAS Ctlg | rs587780147 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587780147(GAGATAA;GAGATAA) |
Alt | rs587780147(GAGATAA;GAGATAA) |
Reference | Rs587780147(-;-) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | RAD50 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.131925377_131925383dupGATAAGA |
CLNSRC | |
CLNACC | RCV000115930.2, |