PLA2G6, phospholipase A2 group VI, 8398

N. diseases: 350; N. variants: 102
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: rs132985
rs132985 		0.827 0.120 22 38167464 intron variant C/T snv 0.51
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2012 2012
dbSNP: rs140758033
rs140758033 		1.000 0.040 22 38112165 missense variant G/C snv 8.6E-04 2.5E-04
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 < 0.001 1 2011 2011
dbSNP: rs2284063
rs2284063 		0.851 0.160 22 38148291 non coding transcript exon variant A/G snv 0.40
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		Nervous System Diseases 0.010 1.000 1 2012 2012