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rs2457174

From SNPedia

Orientationminus
Stabilizedminus
Make rs2457174(A;A)
Make rs2457174(A;G)
Make rs2457174(G;G)
ReferenceGRCh38 38.1/142
Chromosome5
Position133843389
is asnp
is mentioned by
dbSNPrs2457174
ebirs2457174
HLIrs2457174
Exacrs2457174
Varsomers2457174
Maprs2457174
PheGenIrs2457174
hapmaprs2457174
1000 genomesrs2457174
hgdprs2457174
ensemblrs2457174
gopubmedrs2457174
geneviewrs2457174
scholarrs2457174
googlers2457174
pharmgkbrs2457174
gwascentralrs2457174
openSNPrs2457174
23andMers2457174
23andMe allrs2457174
SNP Nexus

SNPshotrs2457174
SNPdbers2457174
MSV3drs2457174
GWAS Ctlgrs2457174
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 7E-8
Odds Ratio NR NR