Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs28939068
CST3
0.790 0.200 20 23635330 missense variant A/T snv 9
rs759304648
GSN
0.790 0.240 9 121312479 synonymous variant G/A snv 8.0E-05 3.5E-05 9
rs1800973
LYZ
0.827 0.320 12 69350234 missense variant C/A snv 4.2E-02 4.3E-02 9
rs11541796
TTR
0.807 0.280 18 31593011 missense variant A/G snv 9
rs79977247
TTR
0.776 0.200 18 31592975 missense variant T/C;G snv 9
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 8
rs63750847
APP
0.790 0.120 21 25897620 missense variant C/T snv 4.5E-04 3.0E-04 8
rs63751039
APP
0.776 0.200 21 25891855 missense variant T/C snv 8
rs140226130
CCDC178
0.790 0.200 18 33336845 intron variant -/CTTTTTGCT delins 7.8E-02 8
rs6656401
CR1
0.776 0.200 1 207518704 intron variant A/G;T snv 8
rs121909715
GSN
0.790 0.160 9 121310819 missense variant G/A;T snv 4.0E-06 8
rs121918094
TTR
0.827 0.280 18 31592921 missense variant T/C snv 8
rs28933981
TTR
0.807 0.200 18 31598647 missense variant C/T snv 1.5E-03 1.7E-03 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
rs73956431
B4GALT6
0.827 0.120 18 31699870 regulatory region variant C/T snv 8.4E-02 6
rs10163755
DSG4 ; DSG1-AS1
0.827 0.200 18 31405413 intron variant G/A snv 0.74 6
rs121909612
FGA
0.807 0.160 4 154585795 missense variant T/A snv 4.0E-06 7.0E-06 6
rs73069071
IAPP ; SLCO1A2
0.807 0.240 12 21357370 intron variant T/C snv 0.14 6
rs387906536
LYZ
0.851 0.200 12 69350215 missense variant T/A;C snv 6
rs370579379
RBP4 ; FFAR4
0.827 0.160 10 93594018 missense variant C/T snv 4.0E-06 1.4E-05 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