WNT3, Wnt family member 3, 7473

N. diseases: 140; N. variants: 22
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: rs415430
rs415430 		1.000 0.040 17 46781778 intron variant C/T snv 0.84
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.800 1.000 2 2011 2011
dbSNP: rs199498
rs199498 		0.925 0.120 17 46788237 intron variant T/C;G snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.800 1.000 1 2014 2014
dbSNP: rs199515
rs199515 		0.925 0.120 17 46779275 intron variant G/C snv 0.84
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.800 1.000 1 2012 2012
dbSNP: rs2074404
rs2074404 		0.925 0.120 17 46788073 intron variant T/G snv 0.27
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.700 1.000 1 2011 2011