Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750959
MAPT
0.827 0.200 17 45962351 missense variant G/A;T snv 6.0E-05 5
rs767543900
MAPT
0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 10
rs1012826460
MAPT
0.925 0.120 17 45971888 missense variant G/A snv 4.0E-06 1.4E-05 2
rs774890160
MAPT
0.925 0.120 17 45974388 missense variant T/C snv 4.2E-06 2
rs1182182524
MAPT
0.882 0.120 17 45983724 missense variant T/G snv 1.4E-05 3
rs1235948930
MAPT
0.882 0.120 17 45983865 missense variant C/T snv 7.0E-06 4
rs760049824
MAPT
0.882 0.120 17 45983867 missense variant T/A;C snv 4.2E-06; 8.5E-06 3
rs751739883
MAPT
0.925 0.120 17 45983891 missense variant C/T snv 4.4E-06 2
rs143624519
MAPT
0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17
rs63750129
MAPT
0.882 0.120 17 45996612 missense variant A/C snv 4.0E-06 4
rs63750349
MAPT
0.851 0.200 17 45996638 missense variant C/G;T snv 4.0E-06 5
rs63750376
MAPT
0.827 0.120 17 45996657 missense variant G/T snv 7
rs63750756
MAPT
0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 23
rs63750416
MAPT
0.851 0.120 17 46010373 missense variant A/C snv 7
rs63751438
MAPT
0.776 0.120 17 46010388 missense variant C/T snv 16
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs63751165
MAPT
0.925 0.120 17 46010401 missense variant G/A;T snv 3
rs63749855
MAPT
0.790 0.200 17 46014271 missense variant T/G snv 8
rs63750635
MAPT
0.851 0.120 17 46014286 missense variant C/T snv 5
rs63750905
MAPT
0.882 0.120 17 46018624 missense variant G/T snv 3
rs63750573
MAPT
0.882 0.120 17 46018627 missense variant A/G snv 3
rs63750570
MAPT
0.827 0.120 17 46018629 missense variant G/A snv 8
rs63750711
MAPT
0.925 0.120 17 46018645 missense variant A/T snv 2
rs63750869
MAPT
0.827 0.160 17 46018707 missense variant G/A snv 2.4E-05 5.6E-05 6
rs63751264
MAPT
0.925 0.120 17 46018726 missense variant A/T snv 2