Gene: MAPT ×
Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1568339995
rs1568339995
MAPT
1 1.000 0.080 17 46018704 missense variant C/T snv 0.700 0
dbSNP: rs143624519
rs143624519
MAPT
17 0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 0.080 0.875 8 2012 2019
dbSNP: rs63750424
rs63750424
MAPT
30 0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 0.080 1.000 8 2002 2019
dbSNP: rs63751273
rs63751273
MAPT
42 0.645 0.280 17 46010389 missense variant C/T snv 0.080 1.000 8 2003 2019
dbSNP: rs242557
rs242557
MAPT
12 0.752 0.200 17 45942346 intron variant G/A snv 0.36 0.060 0.833 6 2008 2017
dbSNP: rs63750570
rs63750570
MAPT
8 0.827 0.120 17 46018629 missense variant G/A snv 0.040 1.000 4 1998 2017
dbSNP: rs2471738
rs2471738
MAPT ; STH
4 0.882 0.160 17 45998697 intron variant C/T snv 0.18 0.030 1.000 3 2009 2017
dbSNP: rs3785883
rs3785883
MAPT
2 0.925 0.080 17 45977067 non coding transcript exon variant A/G snv 0.81 0.030 1.000 3 2014 2018
dbSNP: rs63751438
rs63751438
MAPT
16 0.776 0.120 17 46010388 missense variant C/T snv 0.030 1.000 3 2010 2018
dbSNP: rs63750376
rs63750376
MAPT
7 0.827 0.120 17 45996657 missense variant G/T snv 0.020 0.500 2 2003 2010
dbSNP: rs1050210428
rs1050210428
MAPT
2 0.925 0.120 17 45983258 missense variant G/A snv 0.010 1.000 1 2014 2014
dbSNP: rs1235948930
rs1235948930
MAPT
4 0.882 0.120 17 45983865 missense variant C/T snv 7.0E-06 0.010 1.000 1 2003 2003
dbSNP: rs1429412356
rs1429412356
MAPT
1 1.000 0.080 17 46023989 missense variant G/A snv 7.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs1467967
rs1467967
MAPT
1 1.000 0.080 17 45908813 intron variant G/A snv 0.66 0.010 1.000 1 2017 2017
dbSNP: rs1483785186
rs1483785186
MAPT
1 1.000 0.080 17 45996464 missense variant A/T snv 0.010 1.000 1 2018 2018
dbSNP: rs17649553
rs17649553
MAPT
4 0.882 0.160 17 45917282 intron variant C/T snv 0.14 0.010 1.000 1 2017 2017
dbSNP: rs63749855
rs63749855
MAPT
8 0.790 0.200 17 46014271 missense variant T/G snv 0.010 1.000 1 2019 2019
dbSNP: rs63750072
rs63750072
MAPT
3 1.000 0.080 17 45983493 missense variant A/G snv 4.0E-02 3.8E-02 0.010 1.000 1 2019 2019
dbSNP: rs7521
rs7521
MAPT ; KANSL1
3 0.925 0.080 17 46028029 3 prime UTR variant A/C;G snv 0.010 1.000 1 2018 2018
dbSNP: rs762046989
rs762046989
MAPT
5 0.851 0.200 17 45971867 missense variant C/G snv 8.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs763459583
rs763459583
MAPT
3 0.882 0.080 17 45987045 missense variant A/G;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2013 2013
dbSNP: rs895897745
rs895897745
MAPT
1 1.000 0.080 17 45991503 missense variant C/T snv 4.0E-06 7.0E-06 0.010 < 0.001 1 2004 2004
dbSNP: rs9468
rs9468
MAPT
6 0.882 0.080 17 46024197 3 prime UTR variant T/C snv 0.15 0.14 0.010 1.000 1 2012 2012