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rs9327881

From SNPedia

Orientationplus
Stabilizedplus
Make rs9327881(A;A)
Make rs9327881(A;G)
Make rs9327881(G;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position103389394
is asnp
is mentioned by
dbSNPrs9327881
ebirs9327881
HLIrs9327881
Exacrs9327881
Varsomers9327881
Maprs9327881
PheGenIrs9327881
hapmaprs9327881
1000 genomesrs9327881
hgdprs9327881
ensemblrs9327881
gopubmedrs9327881
geneviewrs9327881
scholarrs9327881
googlers9327881
pharmgkbrs9327881
gwascentralrs9327881
openSNPrs9327881
23andMers9327881
23andMe allrs9327881
SNP Nexus

SNPshotrs9327881
SNPdbers9327881
MSV3drs9327881
GWAS Ctlgrs9327881
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 5E-9
Odds Ratio NR NR