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

rs12817488

From SNPedia

Orientationplus
Stabilizedplus
Make rs12817488(A;A)
Make rs12817488(A;G)
Make rs12817488(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position122811747
GeneCCDC62
is asnp
is mentioned by
dbSNPrs12817488
ebirs12817488
HLIrs12817488
Exacrs12817488
Varsomers12817488
Maprs12817488
PheGenIrs12817488
hapmaprs12817488
1000 genomesrs12817488
hgdprs12817488
ensemblrs12817488
gopubmedrs12817488
geneviewrs12817488
scholarrs12817488
googlers12817488
pharmgkbrs12817488
gwascentralrs12817488
openSNPrs12817488
23andMers12817488
23andMe allrs12817488
SNP Nexus

SNPshotrs12817488
SNPdbers12817488
MSV3drs12817488
GWAS Ctlgrs12817488
GMAF0.3994
Max Magnitude
GWAS snp
PMID [PMID 21292315OA-icon.png]
Trait
Title Imputation of sequence variants for identification of genetic risks for Parkinson's disease: a meta-analysis of genome-wide association studies
Risk Allele T
P-val 3E-13
Odds Ratio 1.1400 [1.10-1.18]

[PMID 25818163] The single nucleotide polymorphism Rs12817488 is associated with Parkinson's disease in the Chinese population