rs4630362
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Geno | Mag | Summary |
|---|---|---|
| (C;C) | 0 | common in complete genomics |
| Make rs4630362(C;G) |
| Make rs4630362(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 104333966 |
| Gene | TXNRD1 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs4630362 |
| dbSNP (classic) | rs4630362 |
| ClinGen | rs4630362 |
| ebi | rs4630362 |
| HLI | rs4630362 |
| Exac | rs4630362 |
| Gnomad | rs4630362 |
| Varsome | rs4630362 |
| LitVar | rs4630362 |
| Map | rs4630362 |
| PheGenI | rs4630362 |
| Biobank | rs4630362 |
| 1000 genomes | rs4630362 |
| hgdp | rs4630362 |
| ensembl | rs4630362 |
| geneview | rs4630362 |
| scholar | rs4630362 |
| rs4630362 | |
| pharmgkb | rs4630362 |
| gwascentral | rs4630362 |
| openSNP | rs4630362 |
| 23andMe | rs4630362 |
| SNPshot | rs4630362 |
| SNPdbe | rs4630362 |
| MSV3d | rs4630362 |
| GWAS Ctlg | rs4630362 |
| GMAF | 0.05234 |
| Max Magnitude | 0 |
| ? | (C;C) (C;G) (G;G) | 28 |
|---|---|---|
|
| ||
[PMID 18996185] rs4630362 is one of several TXNRD1 SNPs significantly associated with familial amyotrophic lateral sclerosis (FALS) but not sporadic amyotrophic lateral sclerosis (ALS).
