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rs4424056

From SNPedia

Orientationplus
Stabilizedplus
Make rs4424056(G;G)
Make rs4424056(G;T)
Make rs4424056(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position91135689
is asnp
is mentioned by
dbSNPrs4424056
ebirs4424056
HLIrs4424056
Exacrs4424056
Varsomers4424056
Maprs4424056
PheGenIrs4424056
hapmaprs4424056
1000 genomesrs4424056
hgdprs4424056
ensemblrs4424056
gopubmedrs4424056
geneviewrs4424056
scholarrs4424056
googlers4424056
pharmgkbrs4424056
gwascentralrs4424056
openSNPrs4424056
23andMers4424056
23andMe allrs4424056
SNP Nexus

SNPshotrs4424056
SNPdbers4424056
MSV3drs4424056
GWAS Ctlgrs4424056
Max Magnitude
? (G;G) (G;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 5E-7
Odds Ratio NR NR