rs17649553, MAPT

N. diseases: 4
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.
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.882 0.160 17 45917282 intron variant C/T snv 0.14 0.720 1.000 4 2014 2019
Corpuscular Hemoglobin Concentration Mean
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
4389 0.882 0.160 17 45917282 intron variant C/T snv 0.14 0.700 1.000 1 2012 2012
Primary biliary cirrhosis
CUI: C0008312
Disease: Primary biliary cirrhosis
667 0.882 0.160 17 45917282 intron variant C/T snv 0.14 0.700 1.000 1 2012 2012
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.882 0.160 17 45917282 intron variant C/T snv 0.14 0.010 1.000 1 2017 2017