Rs121434541
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs121434541 |
| PheGenI | rs121434541 |
| nextbio | rs121434541 |
| hapmap | rs121434541 |
| 1000 genomes | rs121434541 |
| hgdp | rs121434541 |
| ensembl | rs121434541 |
| gopubmed | rs121434541 |
| geneview | rs121434541 |
| scholar | rs121434541 |
| rs121434541 | |
| pharmgkb | rs121434541 |
| gwascentral | rs121434541 |
| openSNP | rs121434541 |
| 23andMe | rs121434541 |
| 23andMe all | rs121434541 |
| SNP Nexus | |
| SNPshot | rs121434541 |
| SNPdbe | rs121434541 |
| MSV3d | rs121434541 |
| Gene | CDH15 |
| Chromosome | 16 |
| Orientation | plus |
| Position | 89249963 |
| Reference | GRCh37 37.1/132 |
| Max Magnitude | 0 |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs121434541(C;T) |
| Make rs121434541(T;T) |
| ClinVar | |
|---|---|
| Risk | rs121434541(T;T) |
| Normal | rs121434541(C;C) |
| Significance | 5 |
| Disease | Mental retardation |
| ClinVar | info |
| Gene | CDH15 |
| CLNDBN | Mental retardation, autosomal dominant 3 |
| Reversed | 0 |
| CLNHGVS | NC_000016.9:g.89249963C>T |
| CLNSRC | OMIM Allelic Variant |
