rs387906812
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs387906812(A;A) |
| Make rs387906812(A;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 22 |
| Position | 23834152 |
| Gene | DERL3, SMARCB1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs387906812 |
| dbSNP (classic) | rs387906812 |
| ClinGen | rs387906812 |
| ebi | rs387906812 |
| HLI | rs387906812 |
| Exac | rs387906812 |
| Gnomad | rs387906812 |
| Varsome | rs387906812 |
| LitVar | rs387906812 |
| Map | rs387906812 |
| PheGenI | rs387906812 |
| Biobank | rs387906812 |
| 1000 genomes | rs387906812 |
| hgdp | rs387906812 |
| ensembl | rs387906812 |
| geneview | rs387906812 |
| scholar | rs387906812 |
| rs387906812 | |
| pharmgkb | rs387906812 |
| gwascentral | rs387906812 |
| openSNP | rs387906812 |
| 23andMe | rs387906812 |
| SNPshot | rs387906812 |
| SNPdbe | rs387906812 |
| MSV3d | rs387906812 |
| GWAS Ctlg | rs387906812 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs387906812(A;A) |
| Alt | rs387906812(A;A) |
| Reference | Rs387906812(G;G) |
| Significance | Pathogenic |
| Disease | Mental retardation |
| Variation | info |
| Gene | DERL3 SMARCB1 |
| CLNDBN | Mental retardation, autosomal dominant 15 |
| Reversed | 0 |
| HGVS | NC_000022.10:g.24176339G>A |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000023124.4, |
