UNC13C, unc-13 homolog C, 440279

N. diseases: 11; N. variants: 5
Disease: Parkinson Disease ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10518765
rs10518765 		1.000 0.040 15 54388434 intron variant A/C snv 0.16
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 1 2006 2006