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rs4761659

From SNPedia

Orientationplus
Stabilizedplus
Make rs4761659(C;C)
Make rs4761659(C;T)
Make rs4761659(T;T)
ReferenceGRCh38 38.1/142
Chromosome12
Position93293308
GeneLOC643339
is asnp
is mentioned by
dbSNPrs4761659
ebirs4761659
HLIrs4761659
Exacrs4761659
Varsomers4761659
Maprs4761659
PheGenIrs4761659
hapmaprs4761659
1000 genomesrs4761659
hgdprs4761659
ensemblrs4761659
gopubmedrs4761659
geneviewrs4761659
scholarrs4761659
googlers4761659
pharmgkbrs4761659
gwascentralrs4761659
openSNPrs4761659
23andMers4761659
23andMe allrs4761659
SNP Nexus

SNPshotrs4761659
SNPdbers4761659
MSV3drs4761659
GWAS Ctlgrs4761659
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-7
Odds Ratio NR NR