Rs10861192
From SNPedia
| is a | snp |
| is | mentioned by |
| dbSNP | rs10861192 |
| hapmap | rs10861192 |
| hgdp | rs10861192 |
| ensembl | rs10861192 |
| gopubmed | rs10861192 |
| scholar | rs10861192 |
| rs10861192 | |
| pharmgkb | rs10861192 |
| hgvbaseg2p | rs10861192 |
| medrefsnp | rs10861192 |
| 23andMe | rs10861192 |
| SNP Nexus |
| Gene | TXNRD1 |
| Chromosome | 12 |
| Orientation | plus |
| Position | 103229553 |
| Genotype | Effect |
|---|---|
| rs10861192(C;C)* | ? |
| rs10861192(C;T)* | ? |
| 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).
