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rs4630362

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs4630362(C;G)
Make rs4630362(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position104333966
GeneTXNRD1
is asnp
is mentioned by
dbSNPrs4630362
ebirs4630362
HLIrs4630362
Exacrs4630362
Varsomers4630362
Maprs4630362
PheGenIrs4630362
hapmaprs4630362
1000 genomesrs4630362
hgdprs4630362
ensemblrs4630362
gopubmedrs4630362
geneviewrs4630362
scholarrs4630362
googlers4630362
pharmgkbrs4630362
gwascentralrs4630362
openSNPrs4630362
23andMers4630362
23andMe allrs4630362
SNP Nexus

SNPshotrs4630362
SNPdbers4630362
MSV3drs4630362
GWAS Ctlgrs4630362
GMAF0.05234
Max Magnitude0
? (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).