Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7224296
rs7224296
NSF ; LRRC37A2
0.882 0.160 17 46722680 intron variant G/A snv 0.59
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 3 2009 2012