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: rs8070723
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy 		0.810 1.000 1 2011 2016
dbSNP: rs8070723
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.800 1.000 5 2009 2014
dbSNP: rs8070723
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial 		0.700 1.000 1 2013 2013
dbSNP: rs8070723
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2012 2012
dbSNP: rs8070723
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012