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rs5029317

From SNPedia

Orientationplus
Stabilizedplus
Make rs5029317(C;C)
Make rs5029317(C;T)
Make rs5029317(T;T)
ReferenceGRCh38 38.1/142
Chromosome8
Position128114607
is asnp
is mentioned by
dbSNPrs5029317
ebirs5029317
HLIrs5029317
Exacrs5029317
Varsomers5029317
Maprs5029317
PheGenIrs5029317
hapmaprs5029317
1000 genomesrs5029317
hgdprs5029317
ensemblrs5029317
gopubmedrs5029317
geneviewrs5029317
scholarrs5029317
googlers5029317
pharmgkbrs5029317
gwascentralrs5029317
openSNPrs5029317
23andMers5029317
23andMe allrs5029317
SNP Nexus

SNPshotrs5029317
SNPdbers5029317
MSV3drs5029317
GWAS Ctlgrs5029317
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 8E-6
Odds Ratio NR NR