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: rs17651549
rs17651549
MAPT
0.882 0.160 17 45983912 missense variant C/T snv 0.15 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.700 1.000 1 2012 2012
dbSNP: rs17651549
rs17651549
MAPT
0.882 0.160 17 45983912 missense variant C/T snv 0.15 0.14
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.700 1.000 1 2012 2012
dbSNP: rs17651549
rs17651549
MAPT
0.882 0.160 17 45983912 missense variant C/T snv 0.15 0.14
CUI: C4083212
Disease: Alopecia, Male Pattern
Alopecia, Male Pattern 		0.700 1.000 1 2012 2012
dbSNP: rs17651549
rs17651549
MAPT
0.882 0.160 17 45983912 missense variant C/T snv 0.15 0.14
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
Corpuscular Hemoglobin Concentration Mean 		0.700 1.000 1 2012 2012