Rs4630362
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs4630362 |
| hapmap | rs4630362 |
| hgdp | rs4630362 |
| ensembl | rs4630362 |
| gopubmed | rs4630362 |
| scholar | rs4630362 |
| rs4630362 | |
| pharmgkb | rs4630362 |
| hgvbaseg2p | rs4630362 |
| medrefsnp | rs4630362 |
| 23andMe | rs4630362 |
| SNP Nexus |
| Gene | TXNRD1 |
| Chromosome | 12 |
| Orientation | plus |
| Position | 103251873 |
| Genotype | Effect |
|---|---|
| rs4630362(C;C)* | ? |
| rs4630362(C;G)* | ? |
| rs4630362(G;G)* | ? |
[PMID 18996185] rs4630362 is one of several TXNRD1 SNPs significantly associated with familial amyotrophic lateral sclerosis (FALS) but not sporadic amyotrophic lateral sclerosis (ALS).
| ? | (C;C) (C;G) (G;G) |
|---|---|
|
| |