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rs947211

From SNPedia

Orientationplus
Stabilizedplus
Make rs947211(A;A)
Make rs947211(A;G)
Make rs947211(G;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position205783537
is asnp
is mentioned by
dbSNPrs947211
ebirs947211
HLIrs947211
Exacrs947211
Varsomers947211
Maprs947211
PheGenIrs947211
hapmaprs947211
1000 genomesrs947211
hgdprs947211
ensemblrs947211
gopubmedrs947211
geneviewrs947211
scholarrs947211
googlers947211
pharmgkbrs947211
gwascentralrs947211
openSNPrs947211
23andMers947211
23andMe allrs947211
SNP Nexus

SNPshotrs947211
SNPdbers947211
MSV3drs947211
GWAS Ctlgrs947211
GMAF0.4298
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19915576]
Trait Parkinson's disease
Title Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease
Risk Allele A
P-val 2E-12
Odds Ratio 1.30 [1.21-1.39]
OMIM613164
Desc
Variant
Relatedalso
[PMID 20413655OA-icon.png] Genetics of neurodegenerative diseases: insights from high-throughput resequencing.


[PMID 21419001] [Association of PARK 16 polymorphisms with Parkinson's disease in Han population of Suzhou area].


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


GET Evidence
rs947211
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.523438
summary



[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.