rs587780150
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs587780150(C;T) |
Make rs587780150(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 5 |
Position | 132589778 |
Gene | RAD50 |
is a | snp |
is | mentioned by |
dbSNP | rs587780150 |
dbSNP (classic) | rs587780150 |
ClinGen | rs587780150 |
ebi | rs587780150 |
HLI | rs587780150 |
Exac | rs587780150 |
Gnomad | rs587780150 |
Varsome | rs587780150 |
LitVar | rs587780150 |
Map | rs587780150 |
PheGenI | rs587780150 |
Biobank | rs587780150 |
1000 genomes | rs587780150 |
hgdp | rs587780150 |
ensembl | rs587780150 |
geneview | rs587780150 |
scholar | rs587780150 |
rs587780150 | |
pharmgkb | rs587780150 |
gwascentral | rs587780150 |
openSNP | rs587780150 |
23andMe | rs587780150 |
SNPshot | rs587780150 |
SNPdbe | rs587780150 |
MSV3d | rs587780150 |
GWAS Ctlg | rs587780150 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587780150(T;T) |
Alt | rs587780150(T;T) |
Reference | Rs587780150(C;C) |
Significance | Pathogenic |
Disease | not provided Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | RAD50 |
CLNDBN | not provided Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.131925470C>T |
CLNSRC | |
CLNACC | RCV000115933.3, RCV000222369.1, |