rs377260382
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs377260382(A;A) |
| Make rs377260382(A;G) |
| Reference | GRCh38 38.1/142 |
| Chromosome | 5 |
| Position | 132557327 |
| Gene | IL5, RAD50 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs377260382 |
| dbSNP (classic) | rs377260382 |
| ClinGen | rs377260382 |
| ebi | rs377260382 |
| HLI | rs377260382 |
| Exac | rs377260382 |
| Gnomad | rs377260382 |
| Varsome | rs377260382 |
| LitVar | rs377260382 |
| Map | rs377260382 |
| PheGenI | rs377260382 |
| Biobank | rs377260382 |
| 1000 genomes | rs377260382 |
| hgdp | rs377260382 |
| ensembl | rs377260382 |
| geneview | rs377260382 |
| scholar | rs377260382 |
| rs377260382 | |
| pharmgkb | rs377260382 |
| gwascentral | rs377260382 |
| openSNP | rs377260382 |
| 23andMe | rs377260382 |
| SNPshot | rs377260382 |
| SNPdbe | rs377260382 |
| MSV3d | rs377260382 |
| GWAS Ctlg | rs377260382 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs377260382(A;A) |
| Alt | rs377260382(A;A) |
| Reference | Rs377260382(G;G) |
| Significance | Other |
| Disease | Hereditary cancer-predisposing syndrome not provided |
| Variation | info |
| Gene | RAD50 IL5 |
| CLNDBN | Hereditary cancer-predisposing syndrome not provided |
| Reversed | 0 |
| HGVS | NC_000005.9:g.131893019G>A |
| CLNSRC | Ambry Genetics ClinVar GeneDx |
| CLNACC | RCV000115961.10, RCV000212899.1, |
