Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1010159 0.882 0.080 11 121612692 non coding transcript exon variant C/T snv 0.55 0.55 3
rs1043202 0.882 0.080 12 54182178 missense variant T/A snv 3
rs1044396 0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
rs104893875 0.742 0.120 4 89828170 missense variant C/T snv 4.0E-06 13
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs104893941 0.776 0.200 5 179836445 missense variant C/T snv 9.8E-04 1.3E-03 9
rs104894002 0.790 0.320 6 41161557 stop gained G/A snv 2.0E-05 2.1E-05 7
rs1057518919 0.851 0.120 14 73171023 missense variant T/G snv 5
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs112451138 0.925 0.080 14 73192667 missense variant T/C snv 7.0E-06 2
rs11669576 0.851 0.160 19 11111624 missense variant G/A snv 4.3E-02 8.4E-02 6
rs11931074 0.851 0.080 4 89718364 intron variant G/A;C;T snv 7
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121909330
VCP
0.752 0.200 9 35065364 missense variant G/A;C;T snv 11
rs121909334
VCP
0.752 0.200 9 35065255 missense variant C/T snv 1.6E-05 10
rs121918100
TTR
0.827 0.160 18 31595184 missense variant T/C snv 11
rs1231783932
APP
0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05 11
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1233347077 0.851 0.160 19 44905894 missense variant G/C snv 7.0E-06 4
rs12604324 1.000 0.080 18 24164468 intron variant G/A snv 0.18 1
rs1289324472
GBA
0.716 0.400 1 155236354 missense variant T/C snv 1.4E-05 21
rs12976445 0.689 0.600 19 51693200 non coding transcript exon variant T/C snv 0.45 20
rs1341026713
APP
0.925 0.080 21 25955719 missense variant G/A snv 4.0E-06 1.4E-05 3
rs1345176461 0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06 40
rs137852642 0.827 0.200 19 15192242 missense variant G/A;T snv 4.5E-06; 4.5E-06 9