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rs3749146

From SNPedia

Orientationplus
Stabilizedplus
Make rs3749146(C;C)
Make rs3749146(C;T)
Make rs3749146(T;T)
ReferenceGRCh38 38.1/142
Chromosome2
Position48597362
GeneSTON1, STON1-GTF2A1L
is asnp
is mentioned by
dbSNPrs3749146
ebirs3749146
HLIrs3749146
Exacrs3749146
Varsomers3749146
Maprs3749146
PheGenIrs3749146
hapmaprs3749146
1000 genomesrs3749146
hgdprs3749146
ensemblrs3749146
gopubmedrs3749146
geneviewrs3749146
scholarrs3749146
googlers3749146
pharmgkbrs3749146
gwascentralrs3749146
openSNPrs3749146
23andMers3749146
23andMe allrs3749146
SNP Nexus

SNPshotrs3749146
SNPdbers3749146
MSV3drs3749146
GWAS Ctlgrs3749146
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 24529757]
Trait Amyotrophic lateral sclerosis (sporadic)
Title A genome-wide association study combining pathway analysis for typical sporadic amyotrophic lateral sclerosis in Chinese Han populations.
Risk Allele
P-val 3E-6
Odds Ratio NR NR