rs878854795
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
Make rs878854795(-;A) |
Make rs878854795(A;A) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 5 |
Position | 132609388 |
Gene | RAD50 |
is a | snp |
is | mentioned by |
dbSNP | rs878854795 |
dbSNP (classic) | rs878854795 |
ClinGen | rs878854795 |
ebi | rs878854795 |
HLI | rs878854795 |
Exac | rs878854795 |
Gnomad | rs878854795 |
Varsome | rs878854795 |
LitVar | rs878854795 |
Map | rs878854795 |
PheGenI | rs878854795 |
Biobank | rs878854795 |
1000 genomes | rs878854795 |
hgdp | rs878854795 |
ensembl | rs878854795 |
geneview | rs878854795 |
scholar | rs878854795 |
rs878854795 | |
pharmgkb | rs878854795 |
gwascentral | rs878854795 |
openSNP | rs878854795 |
23andMe | rs878854795 |
SNPshot | rs878854795 |
SNPdbe | rs878854795 |
MSV3d | rs878854795 |
GWAS Ctlg | rs878854795 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs878854795(A;A) |
Alt | rs878854795(A;A) |
Reference | Rs878854795(-;-) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | RAD50 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.131945080dupA |
CLNSRC | |
CLNACC | RCV000231380.2, |