UNC13C, unc-13 homolog C, 440279

N. diseases: 11; N. variants: 5
Disease: Parkinson Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10518765
rs10518765
Entrez Id: 440279
Gene Symbol: UNC13C
UNC13C
CUI: C0030567
Disease:
Parkinson Disease 		0.700 GeneticVariation GWASDB Genome-wide genotyping in Parkinson's disease and neurologically normal controls: first stage analysis and public release of data. 17052657 2006