rs121909343
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (T;T) | 0 | common in complete genomics |
| Make rs121909343(C;C) |
| Make rs121909343(C;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 2 |
| Position | 74368870 |
| Gene | DCTN1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs121909343 |
| dbSNP (classic) | rs121909343 |
| ClinGen | rs121909343 |
| ebi | rs121909343 |
| HLI | rs121909343 |
| Exac | rs121909343 |
| Gnomad | rs121909343 |
| Varsome | rs121909343 |
| LitVar | rs121909343 |
| Map | rs121909343 |
| PheGenI | rs121909343 |
| Biobank | rs121909343 |
| 1000 genomes | rs121909343 |
| hgdp | rs121909343 |
| ensembl | rs121909343 |
| geneview | rs121909343 |
| scholar | rs121909343 |
| rs121909343 | |
| pharmgkb | rs121909343 |
| gwascentral | rs121909343 |
| openSNP | rs121909343 |
| 23andMe | rs121909343 |
| SNPshot | rs121909343 |
| SNPdbe | rs121909343 |
| MSV3d | rs121909343 |
| GWAS Ctlg | rs121909343 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs121909343(C;C) |
| Alt | rs121909343(C;C) |
| Reference | Rs121909343(T;T) |
| Significance | Other |
| Disease | Amyotrophic lateral sclerosis |
| Variation | info |
| Gene | DCTN1 |
| CLNDBN | Amyotrophic lateral sclerosis, susceptibility to |
| Reversed | 1 |
| HGVS | NC_000002.11:g.74595997A>G |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000008911.2, |
