rs17166050
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs17166050(C;T) |
| Make rs17166050(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 5 |
| Position | 132579521 |
| Gene | RAD50 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs17166050 |
| dbSNP (classic) | rs17166050 |
| ClinGen | rs17166050 |
| ebi | rs17166050 |
| HLI | rs17166050 |
| Exac | rs17166050 |
| Gnomad | rs17166050 |
| Varsome | rs17166050 |
| LitVar | rs17166050 |
| Map | rs17166050 |
| PheGenI | rs17166050 |
| Biobank | rs17166050 |
| 1000 genomes | rs17166050 |
| hgdp | rs17166050 |
| ensembl | rs17166050 |
| geneview | rs17166050 |
| scholar | rs17166050 |
| rs17166050 | |
| pharmgkb | rs17166050 |
| gwascentral | rs17166050 |
| openSNP | rs17166050 |
| 23andMe | rs17166050 |
| SNPshot | rs17166050 |
| SNPdbe | rs17166050 |
| MSV3d | rs17166050 |
| GWAS Ctlg | rs17166050 |
| GMAF | 0.1676 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
|
| ||
[PMID 24093751
] Germline variants in MRE11/RAD50/NBN complex genes in childhood leukemia
[PMID 16724073] Sequence variation, linkage disequilibrium and association with Crohn's disease on chromosome 5q31.
[PMID 26014697] [Association between polymorphism of RAD50 gene and acute lymphoid leukemia in children]
| ClinVar | |
|---|---|
| Risk | rs17166050(T;T) |
| Alt | rs17166050(T;T) |
| Reference | Rs17166050(C;C) |
| Significance | Non-pathogenic |
| Disease | not specified |
| Variation | info |
| Gene | RAD50 |
| CLNDBN | not specified |
| Reversed | 1 |
| HGVS | NC_000005.9:g.131915213G>A |
| CLNSRC | |
| CLNACC | RCV000245201.1, |
