rs587782488
From SNPedia
Merged into | rs587780154 |
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(AAAG;AAAG) | 0 | common in clinvar |
Make rs587782488(-;-) |
Make rs587782488(-;AAAG) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 5 |
Position | 132609340 |
Gene | RAD50 |
is a | snp |
is | mentioned by |
dbSNP | rs587782488 |
dbSNP (classic) | rs587782488 |
ClinGen | rs587782488 |
ebi | rs587782488 |
HLI | rs587782488 |
Exac | rs587782488 |
Gnomad | rs587782488 |
Varsome | rs587782488 |
LitVar | rs587782488 |
Map | rs587782488 |
PheGenI | rs587782488 |
Biobank | rs587782488 |
1000 genomes | rs587782488 |
hgdp | rs587782488 |
ensembl | rs587782488 |
geneview | rs587782488 |
scholar | rs587782488 |
rs587782488 | |
pharmgkb | rs587782488 |
gwascentral | rs587782488 |
openSNP | rs587782488 |
23andMe | rs587782488 |
SNPshot | rs587782488 |
SNPdbe | rs587782488 |
MSV3d | rs587782488 |
GWAS Ctlg | rs587782488 |
Status | Merged into rs587780154 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | |
Alt | |
Reference | Rs587782488(AAAG;AAAG) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | RAD50 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.131945035_131945038delGAAA |
CLNSRC | |
CLNACC | RCV000115951.3, |