Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs63750424
MAPT
0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs143624519
MAPT
0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17
rs63751438
MAPT
0.776 0.120 17 46010388 missense variant C/T snv 16
rs242557
MAPT
0.752 0.200 17 45942346 intron variant G/A snv 0.36 12
rs63749855
MAPT
0.790 0.200 17 46014271 missense variant T/G snv 8
rs63750570
MAPT
0.827 0.120 17 46018629 missense variant G/A snv 8
rs63750376
MAPT
0.827 0.120 17 45996657 missense variant G/T snv 7
rs9468
MAPT
0.882 0.080 17 46024197 3 prime UTR variant T/C snv 0.15 0.14 6
rs762046989
MAPT
0.851 0.200 17 45971867 missense variant C/G snv 8.0E-06 5
rs1235948930
MAPT
0.882 0.120 17 45983865 missense variant C/T snv 7.0E-06 4
rs17649553
MAPT
0.882 0.160 17 45917282 intron variant C/T snv 0.14 4
rs2471738
STH ; MAPT
0.882 0.160 17 45998697 intron variant C/T snv 0.18 4
rs63750072
MAPT
1.000 0.080 17 45983493 missense variant A/G snv 4.0E-02 3.8E-02 3
rs763459583
MAPT
0.882 0.080 17 45987045 missense variant A/G;T snv 4.0E-06; 4.0E-06 3
rs7521
MAPT ; KANSL1
0.925 0.080 17 46028029 3 prime UTR variant A/C;G snv 3
rs1050210428
MAPT
0.925 0.120 17 45983258 missense variant G/A snv 2
rs3785883
MAPT
0.925 0.080 17 45977067 non coding transcript exon variant A/G snv 0.81 2
rs1429412356
MAPT
1.000 0.080 17 46023989 missense variant G/A snv 7.0E-06 1
rs1467967
MAPT
1.000 0.080 17 45908813 intron variant G/A snv 0.66 1
rs1483785186
MAPT
1.000 0.080 17 45996464 missense variant A/T snv 1
rs1568339995
MAPT
1.000 0.080 17 46018704 missense variant C/T snv 1
rs895897745
MAPT
1.000 0.080 17 45991503 missense variant C/T snv 4.0E-06 7.0E-06 1