rs776395588
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs776395588(C;C) |
Make rs776395588(C;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 5 |
Position | 132604038 |
Gene | RAD50 |
is a | snp |
is | mentioned by |
dbSNP | rs776395588 |
dbSNP (classic) | rs776395588 |
ClinGen | rs776395588 |
ebi | rs776395588 |
HLI | rs776395588 |
Exac | rs776395588 |
Gnomad | rs776395588 |
Varsome | rs776395588 |
LitVar | rs776395588 |
Map | rs776395588 |
PheGenI | rs776395588 |
Biobank | rs776395588 |
1000 genomes | rs776395588 |
hgdp | rs776395588 |
ensembl | rs776395588 |
geneview | rs776395588 |
scholar | rs776395588 |
rs776395588 | |
pharmgkb | rs776395588 |
gwascentral | rs776395588 |
openSNP | rs776395588 |
23andMe | rs776395588 |
SNPshot | rs776395588 |
SNPdbe | rs776395588 |
MSV3d | rs776395588 |
GWAS Ctlg | rs776395588 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs776395588(A;A) rs776395588(C;C) |
Alt | rs776395588(A;A) rs776395588(C;C) |
Reference | Rs776395588(T;T) |
Significance | Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | RAD50 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.131939730T>A |
CLNSRC | |
CLNACC | RCV000164879.1, |