Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs1475170339
IGFALS ; SPSB3
0.732 0.240 16 1792325 missense variant T/C;G snv 18
rs121918075
TTR
0.752 0.280 18 31598632 missense variant A/G snv 15
rs121918100
TTR
0.827 0.160 18 31595184 missense variant T/C snv 11
rs572842823
APP
0.763 0.160 21 25897626 missense variant T/A;G snv 11
rs121918079
TTR
0.790 0.280 18 31595143 missense variant T/C snv 10
rs121918097
TTR
0.790 0.280 18 31595137 missense variant G/A snv 10
rs17070145
WWC1
0.790 0.120 5 168418786 intron variant C/T snv 0.43 10
rs63750526
PSEN1
0.776 0.160 14 73192832 missense variant C/A snv 10
rs11541796
TTR
0.807 0.280 18 31593011 missense variant A/G snv 9
rs28939068
CST3
0.790 0.200 20 23635330 missense variant A/T snv 9
rs79977247
TTR
0.776 0.200 18 31592975 missense variant T/C;G snv 9
rs121918094
TTR
0.827 0.280 18 31592921 missense variant T/C snv 8
rs140226130
CCDC178
0.790 0.200 18 33336845 intron variant -/CTTTTTGCT delins 7.8E-02 8
rs63751039
APP
0.776 0.200 21 25891855 missense variant T/C snv 8
rs6656401
CR1
0.776 0.200 1 207518704 intron variant A/G;T snv 8
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 8
rs121913547
LYZ
0.807 0.200 12 69350192 missense variant T/C snv 7
rs121918098
TTR
0.807 0.200 18 31592939 missense variant A/G snv 7
rs10163755
DSG4 ; DSG1-AS1
0.827 0.200 18 31405413 intron variant G/A snv 0.74 6
rs104894664
TTR
0.882 0.120 18 31592959 missense variant G/A snv 6
rs121918068
TTR
0.882 0.200 18 31592983 missense variant T/A;C snv 6
rs121918082
TTR
0.827 0.280 18 31595244 missense variant G/C snv 6
rs387906536
LYZ
0.851 0.200 12 69350215 missense variant T/A;C snv 6
rs73069071
IAPP ; SLCO1A2
0.807 0.240 12 21357370 intron variant T/C snv 0.14 6