rs764122619
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs764122619(C;C) |
Make rs764122619(C;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 5 |
Position | 132580068 |
Gene | RAD50 |
is a | snp |
is | mentioned by |
dbSNP | rs764122619 |
dbSNP (classic) | rs764122619 |
ClinGen | rs764122619 |
ebi | rs764122619 |
HLI | rs764122619 |
Exac | rs764122619 |
Gnomad | rs764122619 |
Varsome | rs764122619 |
LitVar | rs764122619 |
Map | rs764122619 |
PheGenI | rs764122619 |
Biobank | rs764122619 |
1000 genomes | rs764122619 |
hgdp | rs764122619 |
ensembl | rs764122619 |
geneview | rs764122619 |
scholar | rs764122619 |
rs764122619 | |
pharmgkb | rs764122619 |
gwascentral | rs764122619 |
openSNP | rs764122619 |
23andMe | rs764122619 |
SNPshot | rs764122619 |
SNPdbe | rs764122619 |
MSV3d | rs764122619 |
GWAS Ctlg | rs764122619 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs764122619(C;C) |
Alt | rs764122619(C;C) |
Reference | Rs764122619(T;T) |
Significance | Probable-Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | RAD50 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.131915760T>C |
CLNSRC | |
CLNACC | RCV000164601.3, |