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rs7117082

From SNPedia

Orientationplus
Stabilizedplus
Make rs7117082(G;G)
Make rs7117082(G;T)
Make rs7117082(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position133522399
GeneOPCML
is asnp
is mentioned by
dbSNPrs7117082
ebirs7117082
HLIrs7117082
Exacrs7117082
Varsomers7117082
Maprs7117082
PheGenIrs7117082
hapmaprs7117082
1000 genomesrs7117082
hgdprs7117082
ensemblrs7117082
gopubmedrs7117082
geneviewrs7117082
scholarrs7117082
googlers7117082
pharmgkbrs7117082
gwascentralrs7117082
openSNPrs7117082
23andMers7117082
23andMe allrs7117082
SNP Nexus

SNPshotrs7117082
SNPdbers7117082
MSV3drs7117082
GWAS Ctlgrs7117082
Max Magnitude
? (G;G) (G;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-9
Odds Ratio 2.79 [2.04-3.81]