Have questions? Visit https://www.reddit.com/r/SNPedia

rs11248060

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common on affy axiom data
Make rs11248060(C;T)
Make rs11248060(T;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position970571
GeneDGKQ
is asnp
is mentioned by
dbSNPrs11248060
ebirs11248060
HLIrs11248060
Exacrs11248060
Varsomers11248060
Maprs11248060
PheGenIrs11248060
hapmaprs11248060
1000 genomesrs11248060
hgdprs11248060
ensemblrs11248060
gopubmedrs11248060
geneviewrs11248060
scholarrs11248060
googlers11248060
pharmgkbrs11248060
gwascentralrs11248060
openSNPrs11248060
23andMers11248060
23andMe allrs11248060
SNP Nexus

SNPshotrs11248060
SNPdbers11248060
MSV3drs11248060
GWAS Ctlgrs11248060
GMAF0.08678
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20070850OA-icon.png]
Trait Parkinson's disease
Title Genome-Wide Association Study Confirms SNPs in SNCA and the MAPT Region as Common Risk Factors for Parkinson Disease
Risk Allele
P-val 0.000002
Odds Ratio None None


[PMID 22451204OA-icon.png] Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2

GWAS snp
PMID [PMID 22438815OA-icon.png]
Trait
Title Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database.
Risk Allele
P-val 3E-12
Odds Ratio 1.2100 None

[PMID 18985386OA-icon.png] Genomewide association study for susceptibility genes contributing to familial Parkinson disease.

[PMID 21281506OA-icon.png] A unified framework for multi-locus association analysis of both common and rare variants.


[PMID 23618683] GAK rs1564282 and DGKQ rs11248060 increase the risk for Parkinson's disease in a Chinese population.