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

rs2281983

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs2281983(C;T)
Make rs2281983(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position102231624
GenePITX3
is asnp
is mentioned by
dbSNPrs2281983
ebirs2281983
HLIrs2281983
Exacrs2281983
Varsomers2281983
Maprs2281983
PheGenIrs2281983
hapmaprs2281983
1000 genomesrs2281983
hgdprs2281983
ensemblrs2281983
gopubmedrs2281983
geneviewrs2281983
scholarrs2281983
googlers2281983
pharmgkbrs2281983
gwascentralrs2281983
openSNPrs2281983
23andMers2281983
23andMe allrs2281983
SNP Nexus

SNPshotrs2281983
SNPdbers2281983
MSV3drs2281983
GWAS Ctlgrs2281983
GMAF0.3118
Max Magnitude0

[PMID 21524731] PITX3 gene polymorphism is associated with Parkinson's disease in Chinese population


[PMID 21565251] Genetic variants of the PITX3 gene are not associated with late-onset sporadic Parkinson's disease in a Chinese population


[PMID 22411443] A novel synonymous SNP in PITX3 is associated with Parkinson's disease in Chinese population


[PMID 19394114] Transcription factor PITX3 gene in Parkinson's disease.


[PMID 19754401OA-icon.png] The role of transcription factor Pitx3 in dopamine neuron development and Parkinson's disease.


[PMID 22037506] PITX3 polymorphism is not associated with Parkinson's disease in a Chinese population.


[PMID 22429667] Meta-analysis of association between PITX3 gene polymorphism and Parkinson's disease.


[PMID 24525476] PITX3 and Risk for Parkinson's Disease: A Systematic Review and Meta-Analysis


ClinVar
Risk rs2281983(T;T)
Alt rs2281983(T;T)
Reference rs2281983(C;C)
Significance Non-pathogenic
Disease not specified
Variation info
Gene PITX3
CLNDBN not specified
Reversed 1
HGVS NC_000010.10:g.103991381G>A
CLNSRC
CLNACC RCV000177223.1,