rs1060501970
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs1060501970(A;C) |
Make rs1060501970(C;C) |
Reference | GRCh38.p7 38.3/150 |
Chromosome | 5 |
Position | 132579860 |
Gene | RAD50 |
is a | snp |
is | mentioned by |
dbSNP | rs1060501970 |
dbSNP (classic) | rs1060501970 |
ClinGen | rs1060501970 |
ebi | rs1060501970 |
HLI | rs1060501970 |
Exac | rs1060501970 |
Gnomad | rs1060501970 |
Varsome | rs1060501970 |
LitVar | rs1060501970 |
Map | rs1060501970 |
PheGenI | rs1060501970 |
Biobank | rs1060501970 |
1000 genomes | rs1060501970 |
hgdp | rs1060501970 |
ensembl | rs1060501970 |
geneview | rs1060501970 |
scholar | rs1060501970 |
rs1060501970 | |
pharmgkb | rs1060501970 |
gwascentral | rs1060501970 |
openSNP | rs1060501970 |
23andMe | rs1060501970 |
SNPshot | rs1060501970 |
SNPdbe | rs1060501970 |
MSV3d | rs1060501970 |
GWAS Ctlg | rs1060501970 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs1060501970(C;C) |
Alt | rs1060501970(C;C) |
Reference | Rs1060501970(A;A) |
Significance | Probable-Pathogenic |
Disease | Hereditary cancer-predisposing syndrome |
Variation | info |
Gene | RAD50 |
CLNDBN | Hereditary cancer-predisposing syndrome |
Reversed | 0 |
HGVS | NC_000005.9:g.131915552A>C |
CLNSRC | |
CLNACC | RCV000458636.1, |