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rs2492937

From SNPedia

Orientationplus
Stabilizedplus
Make rs2492937(A;A)
Make rs2492937(A;G)
Make rs2492937(G;G)
ReferenceGRCh38 38.1/142
Chromosome6
Position42086608
is asnp
is mentioned by
dbSNPrs2492937
ebirs2492937
HLIrs2492937
Exacrs2492937
Varsomers2492937
Maprs2492937
PheGenIrs2492937
hapmaprs2492937
1000 genomesrs2492937
hgdprs2492937
ensemblrs2492937
gopubmedrs2492937
geneviewrs2492937
scholarrs2492937
googlers2492937
pharmgkbrs2492937
gwascentralrs2492937
openSNPrs2492937
23andMers2492937
23andMe allrs2492937
SNP Nexus

SNPshotrs2492937
SNPdbers2492937
MSV3drs2492937
GWAS Ctlgrs2492937
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 6E-6
Odds Ratio NR NR