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rs9329300

From SNPedia

Orientationplus
Stabilizedplus
Make rs9329300(A;A)
Make rs9329300(A;C)
Make rs9329300(C;C)
ReferenceGRCh38 38.1/142
Chromosome10
Position2747402
is asnp
is mentioned by
dbSNPrs9329300
ebirs9329300
HLIrs9329300
Exacrs9329300
Varsomers9329300
Maprs9329300
PheGenIrs9329300
hapmaprs9329300
1000 genomesrs9329300
hgdprs9329300
ensemblrs9329300
gopubmedrs9329300
geneviewrs9329300
scholarrs9329300
googlers9329300
pharmgkbrs9329300
gwascentralrs9329300
openSNPrs9329300
23andMers9329300
23andMe allrs9329300
SNP Nexus

SNPshotrs9329300
SNPdbers9329300
MSV3drs9329300
GWAS Ctlgrs9329300
Max Magnitude
? (A;A) (A;C) (C;C) 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 2E-9
Odds Ratio 3.10 [2.25-4.27]