Rs11203289
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs11203289 |
| PheGenI | rs11203289 |
| nextbio | rs11203289 |
| hapmap | rs11203289 |
| 1000 genomes | rs11203289 |
| hgdp | rs11203289 |
| ensembl | rs11203289 |
| gopubmed | rs11203289 |
| geneview | rs11203289 |
| scholar | rs11203289 |
| rs11203289 | |
| pharmgkb | rs11203289 |
| gwascentral | rs11203289 |
| openSNP | rs11203289 |
| 23andMe | rs11203289 |
| 23andMe all | rs11203289 |
| SNP Nexus | |
| SNPshot | rs11203289 |
| SNPdbe | rs11203289 |
| MSV3d | rs11203289 |
| Gene | SDHB |
| Chromosome | 1 |
| Orientation | plus |
| Position | 17380507 |
| Reference | GRCh37 37.1/132 |
| Max Magnitude | 0 |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| (G;G) | 0 | common in complete genomics |
| Make rs11203289(C;G) |
| ClinVar | |
|---|---|
| Risk | rs11203289(G;G) |
| Normal | rs11203289(C;C) |
| Significance | 5 |
| Disease | Cowden-like syndrome |
| ClinVar | info |
| Gene | SDHB |
| CLNDBN | Cowden-like syndrome |
| Reversed | 1 |
| CLNHGVS | NC_000001.10:g.17380507G>C |
| CLNSRC | OMIM Allelic Variant |