Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs1595014 0.882 0.120 7 12148903 intergenic variant T/A snv 0.23 3
rs1205185774
AHSA1
0.882 0.120 14 77469161 missense variant C/T snv 4
rs781049584
APP
0.724 0.280 21 26021917 missense variant T/G snv 8.2E-06 7.0E-06 18
rs1386984902
APP
0.790 0.160 21 26000095 missense variant G/A snv 9
rs63750066
APP
0.763 0.160 21 25891796 missense variant C/T snv 9.5E-05 6.3E-05 9
rs5848
FAM171A2 ; GRN
0.708 0.120 17 44352876 3 prime UTR variant C/T snv 0.41 17
rs63751294
GRN
0.827 0.120 17 44352404 stop gained C/T snv 8.0E-06 6
rs9897526
GRN
0.925 0.120 17 44349572 non coding transcript exon variant G/A;C snv 0.16 2
rs1189501362
GSK3B
0.882 0.120 3 119863583 missense variant G/A snv 7.0E-06 4
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs866604606
MAPK1
0.882 0.120 22 21772907 missense variant G/A snv 4
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
rs63750756
MAPT
0.716 0.200 17 46010324 missense variant T/G snv 2.6E-05 23
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
rs767543900
MAPT
0.790 0.120 17 45971879 missense variant A/C;G snv 4.0E-06 10
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
rs63750416
MAPT
0.851 0.120 17 46010373 missense variant A/C snv 7
rs63750512
MAPT
0.827 0.160 17 46024010 missense variant G/A;C snv 1.2E-05 6
rs63750869
MAPT
0.827 0.160 17 46018707 missense variant G/A snv 2.4E-05 5.6E-05 6
rs63750349
MAPT
0.851 0.200 17 45996638 missense variant C/G;T snv 4.0E-06 5