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rs4824093

From SNPedia

Orientationplus
Stabilizedplus
Make rs4824093(A;A)
Make rs4824093(A;G)
Make rs4824093(G;G)
ReferenceGRCh38 38.1/142
Chromosome22
Position49734620
is asnp
is mentioned by
dbSNPrs4824093
ebirs4824093
HLIrs4824093
Exacrs4824093
Varsomers4824093
Maprs4824093
PheGenIrs4824093
hapmaprs4824093
1000 genomesrs4824093
hgdprs4824093
ensemblrs4824093
gopubmedrs4824093
geneviewrs4824093
scholarrs4824093
googlers4824093
pharmgkbrs4824093
gwascentralrs4824093
openSNPrs4824093
23andMers4824093
23andMe allrs4824093
SNP Nexus

SNPshotrs4824093
SNPdbers4824093
MSV3drs4824093
GWAS Ctlgrs4824093
Max Magnitude
? (A;A) (A;G) (G;G) 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 8E-6
Odds Ratio NR NR