rs587781625
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs587781625(-;A) |
Make rs587781625(A;A) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 5 |
Position | 132557418 |
Gene | IL5, RAD50 |
is a | snp |
is | mentioned by |
dbSNP | rs587781625 |
dbSNP (classic) | rs587781625 |
ClinGen | rs587781625 |
ebi | rs587781625 |
HLI | rs587781625 |
Exac | rs587781625 |
Gnomad | rs587781625 |
Varsome | rs587781625 |
LitVar | rs587781625 |
Map | rs587781625 |
PheGenI | rs587781625 |
Biobank | rs587781625 |
1000 genomes | rs587781625 |
hgdp | rs587781625 |
ensembl | rs587781625 |
geneview | rs587781625 |
scholar | rs587781625 |
rs587781625 | |
pharmgkb | rs587781625 |
gwascentral | rs587781625 |
openSNP | rs587781625 |
23andMe | rs587781625 |
SNPshot | rs587781625 |
SNPdbe | rs587781625 |
MSV3d | rs587781625 |
GWAS Ctlg | rs587781625 |
Merged from | Rs867328327 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587781625(A;A) |
Alt | rs587781625(A;A) |
Reference | Rs587781625(-;-) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | RAD50 IL5 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.131893110dupA |
CLNSRC | |
CLNACC | RCV000129727.4, |