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rs2322978

From SNPedia

Orientationplus
Stabilizedplus
Make rs2322978(A;A)
Make rs2322978(A;G)
Make rs2322978(G;G)
ReferenceGRCh38 38.1/142
Chromosome11
Position127846245
is asnp
is mentioned by
dbSNPrs2322978
ebirs2322978
HLIrs2322978
Exacrs2322978
Varsomers2322978
Maprs2322978
PheGenIrs2322978
hapmaprs2322978
1000 genomesrs2322978
hgdprs2322978
ensemblrs2322978
gopubmedrs2322978
geneviewrs2322978
scholarrs2322978
googlers2322978
pharmgkbrs2322978
gwascentralrs2322978
openSNPrs2322978
23andMers2322978
23andMe allrs2322978
SNP Nexus

SNPshotrs2322978
SNPdbers2322978
MSV3drs2322978
GWAS Ctlgrs2322978
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 8E-7
Odds Ratio NR NR