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

rs2338971

From SNPedia

Orientationplus
Stabilizedplus
Make rs2338971(C;C)
Make rs2338971(C;T)
Make rs2338971(T;T)
ReferenceGRCh38 38.1/142
Chromosome1
Position101414449
is asnp
is mentioned by
dbSNPrs2338971
ebirs2338971
HLIrs2338971
Exacrs2338971
Varsomers2338971
Maprs2338971
PheGenIrs2338971
hapmaprs2338971
1000 genomesrs2338971
hgdprs2338971
ensemblrs2338971
gopubmedrs2338971
geneviewrs2338971
scholarrs2338971
googlers2338971
pharmgkbrs2338971
gwascentralrs2338971
openSNPrs2338971
23andMers2338971
23andMe allrs2338971
SNP Nexus

SNPshotrs2338971
SNPdbers2338971
MSV3drs2338971
GWAS Ctlgrs2338971
Max Magnitude
GWAS snp
PMID [PMID 24511991OA-icon.png]
Trait Parkinson's disease
Title Identification of a novel Parkinson's disease locus via stratified genome-wide association study.
Risk Allele C
P-val 5E-10
Odds Ratio 1.32 [1.26-1.38]