rs121912442
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in clinvar |
| Make rs121912442(C;T) |
| Make rs121912442(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 21 |
| Position | 31659783 |
| Gene | LOC102724449, SOD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs121912442 |
| dbSNP (classic) | rs121912442 |
| ClinGen | rs121912442 |
| ebi | rs121912442 |
| HLI | rs121912442 |
| Exac | rs121912442 |
| Gnomad | rs121912442 |
| Varsome | rs121912442 |
| LitVar | rs121912442 |
| Map | rs121912442 |
| PheGenI | rs121912442 |
| Biobank | rs121912442 |
| 1000 genomes | rs121912442 |
| hgdp | rs121912442 |
| ensembl | rs121912442 |
| geneview | rs121912442 |
| scholar | rs121912442 |
| rs121912442 | |
| pharmgkb | rs121912442 |
| gwascentral | rs121912442 |
| openSNP | rs121912442 |
| 23andMe | rs121912442 |
| SNPshot | rs121912442 |
| SNPdbe | rs121912442 |
| MSV3d | rs121912442 |
| GWAS Ctlg | rs121912442 |
| Max Magnitude | 0 |
| ClinVar | |
|---|---|
| Risk | rs121912442(T;T) |
| Alt | rs121912442(T;T) |
| Reference | Rs121912442(C;C) |
| Significance | Pathogenic |
| Disease | Amyotrophic lateral sclerosis type 1 |
| Variation | info |
| Gene | SOD1 |
| CLNDBN | Amyotrophic lateral sclerosis type 1 |
| Reversed | 0 |
| HGVS | NC_000021.8:g.33032096C>T |
| CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
| CLNACC | RCV000015885.27, |
A polymorphism on the SOD1 gene known as A4V.
