Rs10861192
From SNPedia
| Orientation | plus |
| is a | snp |
| is | mentioned by |
| dbSNP | rs10861192 |
| PheGenI | rs10861192 |
| nextbio | rs10861192 |
| hapmap | rs10861192 |
| 1000 genomes | rs10861192 |
| hgdp | rs10861192 |
| ensembl | rs10861192 |
| gopubmed | rs10861192 |
| geneview | rs10861192 |
| scholar | rs10861192 |
| rs10861192 | |
| pharmgkb | rs10861192 |
| gwascentral | rs10861192 |
| openSNP | rs10861192 |
| 23andMe | rs10861192 |
| 23andMe all | rs10861192 |
| SNP Nexus | |
| SNPshot | rs10861192 |
| SNPdbe | rs10861192 |
| MSV3d | rs10861192 |
| Gene | TXNRD1 |
| Chromosome | 12 |
| Orientation | plus |
| GMAF | 0.4936 |
| Position | 104705424 |
| Reference | GRCh37 37.1/131 |
| Max Magnitude |
| Make rs10861192(C;C) |
| Make rs10861192(C;T) |
| Make rs10861192(T;T) |
[PMID 18996185] rs10861192 is one of several TXNRD1 SNPs significantly associated with familial amyotrophic lateral sclerosis (FALS) but not sporadic amyotrophic lateral sclerosis (ALS).
