rs8070723, MAPT

N. diseases: 7
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Progressive supranuclear palsy
CUI: C0038868
Disease: Progressive supranuclear palsy
52 0.851 0.240 17 46003698 intron variant A/G snv 0.18 0.810 1.000 2 2011 2016
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.851 0.240 17 46003698 intron variant A/G snv 0.18 0.800 1.000 5 2009 2014
Corpuscular Hemoglobin Concentration Mean
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
4389 0.851 0.240 17 46003698 intron variant A/G snv 0.18 0.700 1.000 1 2012 2012
Lung Diseases, Interstitial
CUI: C0206062
Disease: Lung Diseases, Interstitial
144 0.851 0.240 17 46003698 intron variant A/G snv 0.18 0.700 1.000 1 2013 2013
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.851 0.240 17 46003698 intron variant A/G snv 0.18 0.700 1.000 1 2012 2012
Waist-Hip Ratio
CUI: C0205682
Disease: Waist-Hip Ratio
1138 0.851 0.240 17 46003698 intron variant A/G snv 0.18 0.700 1.000 1 2019 2019
Behavioral variant of frontotemporal dementia
CUI: C4011788
Disease: Behavioral variant of frontotemporal dementia
10 0.851 0.240 17 46003698 intron variant A/G snv 0.18 0.010 1.000 1 2014 2014