Source: GWASCAT

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: rs242557
rs242557
MAPT
0.752 0.200 17 45942346 intron variant G/A snv 0.36
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy 		0.860 1.000 2 2010 2019
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: rs17564829
rs17564829
MAPT ; LOC105371800
1.000 0.080 17 45929235 intron variant T/C snv 0.14
CUI: C0008312
Disease: Primary biliary cirrhosis
Primary biliary cirrhosis 		0.800 1.000 1 2012 2012
dbSNP: rs1981997
rs1981997
MAPT
1.000 0.040 17 45979401 non coding transcript exon variant G/A snv 0.14
CUI: C0206062
Disease: Lung Diseases, Interstitial
Lung Diseases, Interstitial 		0.800 1.000 1 2013 2013
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 1 2009 2014
dbSNP: rs17649553
rs17649553
MAPT
0.882 0.160 17 45917282 intron variant C/T snv 0.14
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.720 1.000 2 2014 2019
dbSNP: rs2471738
rs2471738
MAPT ; STH
0.882 0.160 17 45998697 intron variant C/T snv 0.18
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 2 2018 2018
dbSNP: rs1052553
rs1052553
MAPT
0.827 0.200 17 45996523 synonymous variant A/G snv 0.14 0.15
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.700 1.000 1 2015 2015
dbSNP: rs112385572
rs112385572
MAPT
1.000 0.080 17 45988806 intron variant A/G snv 0.15
CUI: C0002170
Disease: Alopecia
Alopecia 		0.700 1.000 1 2017 2017
dbSNP: rs141455452
rs141455452
MAPT
17 45941717 intron variant T/C;G snv
CUI: C0008074
Disease: Child Development Disorders, Pervasive
Child Development Disorders, Pervasive 		0.700 1.000 1 2019 2019
dbSNP: rs1560312
rs1560312
MAPT
1.000 0.040 17 45901622 intron variant A/G snv 0.29
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs1560312
rs1560312
MAPT
1.000 0.040 17 45901622 intron variant A/G snv 0.29
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs17563986
rs17563986
MAPT
1.000 0.040 17 45913906 intron variant A/G snv 0.14
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2017 2017
dbSNP: rs17651507
rs17651507
MAPT
17 45981644 intron variant A/T snv 0.20
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio 		0.700 1.000 1 2019 2019
dbSNP: rs1864325
rs1864325
MAPT
0.882 0.160 17 45900461 intron variant C/T snv 0.14
CUI: C0005938
Disease: Bone Density
Bone Density 		0.700 1.000 1 2012 2012
dbSNP: rs1991556
rs1991556
MAPT
1.000 0.040 17 46006036 intron variant G/A snv 0.14
CUI: C0042834
Disease: Vital capacity
Vital capacity 		0.700 1.000 1 2019 2019
dbSNP: rs1991556
rs1991556
MAPT
1.000 0.040 17 46006036 intron variant G/A snv 0.14
CUI: C0424574
Disease: Duration of sleep
Duration of sleep 		0.700 1.000 1 2018 2018
dbSNP: rs242557
rs242557
MAPT
0.752 0.200 17 45942346 intron variant G/A snv 0.36
CUI: C0004238
Disease: Atrial Fibrillation
Atrial Fibrillation 		0.700 1.000 1 2018 2018
dbSNP: rs242559
rs242559
MAPT
1.000 0.080 17 45948522 intron variant C/A snv 0.71
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs242562
rs242562
MAPT
1.000 0.040 17 45949373 intron variant G/A snv 0.35
CUI: C0429097
Disease: QRS complex feature
QRS complex feature 		0.700 1.000 1 2016 2016
dbSNP: rs2435200
rs2435200
MAPT
0.925 0.080 17 45994485 intron variant G/A snv 0.40
CUI: C1269683
Disease: Major Depressive Disorder
Major Depressive Disorder 		0.700 1.000 1 2018 2018
dbSNP: rs2435200
rs2435200
MAPT
0.925 0.080 17 45994485 intron variant G/A snv 0.40
CUI: C0525045
Disease: Mood Disorders
Mood Disorders 		0.700 1.000 1 2018 2018
dbSNP: rs2435210
rs2435210
MAPT
1.000 0.040 17 45984528 intron variant C/T snv 0.29
CUI: C0003467
Disease: Anxiety
Anxiety 		0.700 1.000 1 2018 2018
dbSNP: rs28646281
rs28646281
MAPT
17 45900480 intron variant T/C;G snv
CUI: C0021704
Disease: Intelligence
Intelligence 		0.700 1.000 1 2018 2018
dbSNP: rs3785879
rs3785879
MAPT
1.000 0.040 17 45908270 non coding transcript exon variant C/A;G;T snv
CUI: C0003467
Disease: Anxiety
Anxiety 		0.700 1.000 1 2018 2018