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: rs62063857
rs62063857
MAPT ; STH
0.882 0.120 17 45999299 missense variant A/G snv 0.14 0.15
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.730 0.750 1 2010 2017
dbSNP: rs62063857
rs62063857
MAPT ; STH
0.882 0.120 17 45999299 missense variant A/G snv 0.14 0.15
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2012 2012