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: rs7846412
rs7846412
PIP4P2
1.000 0.040 8 91032300 intron variant A/G snv 0.47
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2006 2006