rs786201531
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs786201531(-;T) |
Make rs786201531(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 5 |
Position | 132579492 |
Gene | RAD50 |
is a | snp |
is | mentioned by |
dbSNP | rs786201531 |
dbSNP (classic) | rs786201531 |
ClinGen | rs786201531 |
ebi | rs786201531 |
HLI | rs786201531 |
Exac | rs786201531 |
Gnomad | rs786201531 |
Varsome | rs786201531 |
LitVar | rs786201531 |
Map | rs786201531 |
PheGenI | rs786201531 |
Biobank | rs786201531 |
1000 genomes | rs786201531 |
hgdp | rs786201531 |
ensembl | rs786201531 |
geneview | rs786201531 |
scholar | rs786201531 |
rs786201531 | |
pharmgkb | rs786201531 |
gwascentral | rs786201531 |
openSNP | rs786201531 |
23andMe | rs786201531 |
SNPshot | rs786201531 |
SNPdbe | rs786201531 |
MSV3d | rs786201531 |
GWAS Ctlg | rs786201531 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs786201531(T;T) |
Alt | rs786201531(T;T) |
Reference | Rs786201531(-;-) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | RAD50 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.131915184dupT |
CLNSRC | |
CLNACC | RCV000163823.4, |