rs750586158
From SNPedia
					| Orientation | plus | 
| Stabilized | plus | 
| Geno | Mag | Summary | 
|---|---|---|
| (C;C) | 0 | common in clinvar | 
| Make rs750586158(C;T) | 
| Make rs750586158(T;T) | 
| Reference | GRCh38.p2 38.2/144 | 
| Chromosome | 5 | 
| Position | 132638203 | 
| Gene | RAD50, TH2LCRR | 
| is a | snp | 
| is | mentioned by | 
| dbSNP | rs750586158 | 
| dbSNP (classic) | rs750586158 | 
| ClinGen | rs750586158 | 
| ebi | rs750586158 | 
| HLI | rs750586158 | 
| Exac | rs750586158 | 
| Gnomad | rs750586158 | 
| Varsome | rs750586158 | 
| LitVar | rs750586158 | 
| Map | rs750586158 | 
| PheGenI | rs750586158 | 
| Biobank | rs750586158 | 
| 1000 genomes | rs750586158 | 
| hgdp | rs750586158 | 
| ensembl | rs750586158 | 
| geneview | rs750586158 | 
| scholar | rs750586158 | 
| rs750586158 | |
| pharmgkb | rs750586158 | 
| gwascentral | rs750586158 | 
| openSNP | rs750586158 | 
| 23andMe | rs750586158 | 
| SNPshot | rs750586158 | 
| SNPdbe | rs750586158 | 
| MSV3d | rs750586158 | 
| GWAS Ctlg | rs750586158 | 
| Max Magnitude | 0 | 
| ClinVar | |
|---|---|
| Risk | rs750586158(T;T) | 
| Alt | rs750586158(T;T) | 
| Reference | Rs750586158(C;C) | 
| Significance | Pathogenic | 
| Disease | Hereditary cancer-predisposing syndrome | 
| Variation | info | 
| Gene | LOC101927761 TH2LCRR RAD50 | 
| CLNDBN | Hereditary cancer-predisposing syndrome | 
| Reversed | 0 | 
| HGVS | NC_000005.9:g.131973895C>T | 
| CLNSRC | |
| CLNACC | RCV000164215.3, | 


