rs104894786
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;G) | 0 | common in clinvar |
| Make rs104894786(G;T) |
| Make rs104894786(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | X |
| Position | 111410188 |
| Gene | DCX |
| is a | snp |
| is | mentioned by |
| dbSNP | rs104894786 |
| dbSNP (classic) | rs104894786 |
| ClinGen | rs104894786 |
| ebi | rs104894786 |
| HLI | rs104894786 |
| Exac | rs104894786 |
| Gnomad | rs104894786 |
| Varsome | rs104894786 |
| LitVar | rs104894786 |
| Map | rs104894786 |
| PheGenI | rs104894786 |
| Biobank | rs104894786 |
| 1000 genomes | rs104894786 |
| hgdp | rs104894786 |
| ensembl | rs104894786 |
| geneview | rs104894786 |
| scholar | rs104894786 |
| rs104894786 | |
| pharmgkb | rs104894786 |
| gwascentral | rs104894786 |
| openSNP | rs104894786 |
| 23andMe | rs104894786 |
| SNPshot | rs104894786 |
| SNPdbe | rs104894786 |
| MSV3d | rs104894786 |
| GWAS Ctlg | rs104894786 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs104894786(T;T) |
| Alt | rs104894786(T;T) |
| Reference | Rs104894786(G;G) |
| Significance | Pathogenic |
| Disease | Lissencephaly Subcortical laminar heterotopia |
| Variation | info |
| Gene | DCX |
| CLNDBN | Lissencephaly, X-linked Subcortical laminar heterotopia, X-linked |
| Reversed | 1 |
| HGVS | NC_000023.10:g.110653416C>A |
| CLNSRC | OMIM Allelic Variant |
| CLNACC | RCV000012375.14, RCV000012376.16, |
