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rs823156

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs823156(A;G)
Make rs823156(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position205795512
GeneSLC41A1
is asnp
is mentioned by
dbSNPrs823156
ebirs823156
HLIrs823156
Exacrs823156
Varsomers823156
Maprs823156
PheGenIrs823156
hapmaprs823156
1000 genomesrs823156
hgdprs823156
ensemblrs823156
gopubmedrs823156
geneviewrs823156
scholarrs823156
googlers823156
pharmgkbrs823156
gwascentralrs823156
openSNPrs823156
23andMers823156
23andMe allrs823156
SNP Nexus

SNPshotrs823156
SNPdbers823156
MSV3drs823156
GWAS Ctlgrs823156
GMAF0.3118
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21738487OA-icon.png]
Trait
Title Web-based genome-wide association study identifies two novel Loci and a substantial genetic component for Parkinson's disease.
Risk Allele A
P-val 1E-7
Odds Ratio 1.2100 [1.12-1.30]
OMIM613164
Desc
Variant
Relatedalso
[PMID 19915575OA-icon.png] Genome-wide association study reveals genetic risk underlying Parkinson's disease.


[PMID 21268244] Association of GWAS loci with PD in China.


[PMID 21840748] An association between the PARK16 locus and Parkinson's disease in a cohort from eastern China.


[PMID 26944116] PARK16 polymorphisms, interaction with smoking, and sporadic Parkinson's disease in Japan.


[PMID 27174169] PARK16 is associated with PD in the Malaysian population.