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rs11167260

From SNPedia

Orientationplus
Stabilizedplus
Make rs11167260(A;A)
Make rs11167260(A;G)
Make rs11167260(G;G)
ReferenceGRCh38 38.1/141
Chromosome20
Position35187397
GenePROCR
is asnp
is mentioned by
dbSNPrs11167260
ebirs11167260
HLIrs11167260
Exacrs11167260
Varsomers11167260
Maprs11167260
PheGenIrs11167260
hapmaprs11167260
1000 genomesrs11167260
hgdprs11167260
ensemblrs11167260
gopubmedrs11167260
geneviewrs11167260
scholarrs11167260
googlers11167260
pharmgkbrs11167260
gwascentralrs11167260
openSNPrs11167260
23andMers11167260
23andMe allrs11167260
SNP Nexus

SNPshotrs11167260
SNPdbers11167260
MSV3drs11167260
GWAS Ctlgrs11167260
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 4E-6
Odds Ratio NR NR