rs587781576
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs587781576(C;T) |
Make rs587781576(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 5 |
Position | 132579953 |
Gene | RAD50 |
is a | snp |
is | mentioned by |
dbSNP | rs587781576 |
dbSNP (classic) | rs587781576 |
ClinGen | rs587781576 |
ebi | rs587781576 |
HLI | rs587781576 |
Exac | rs587781576 |
Gnomad | rs587781576 |
Varsome | rs587781576 |
LitVar | rs587781576 |
Map | rs587781576 |
PheGenI | rs587781576 |
Biobank | rs587781576 |
1000 genomes | rs587781576 |
hgdp | rs587781576 |
ensembl | rs587781576 |
geneview | rs587781576 |
scholar | rs587781576 |
rs587781576 | |
pharmgkb | rs587781576 |
gwascentral | rs587781576 |
openSNP | rs587781576 |
23andMe | rs587781576 |
SNPshot | rs587781576 |
SNPdbe | rs587781576 |
MSV3d | rs587781576 |
GWAS Ctlg | rs587781576 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587781576(T;T) |
Alt | rs587781576(T;T) |
Reference | Rs587781576(C;C) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | RAD50 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.131915645C>T |
CLNSRC | |
CLNACC | RCV000129612.2, |