Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 70
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 36
rs267607161
TTR
0.742 0.360 18 31598580 missense variant G/T snv 4.0E-06 7.0E-06 16
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
rs786201856
APC
0.776 0.200 5 112815507 stop gained C/T snv 10
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
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
rs140226130
CCDC178
0.790 0.200 18 33336845 intron variant -/CTTTTTGCT delins 7.8E-02 8
rs121918090
TTR
0.790 0.240 18 31593026 missense variant G/C snv 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
rs121918098
TTR
0.807 0.200 18 31592939 missense variant A/G snv 7
rs766001707
ATXN3
0.851 0.200 14 92096772 missense variant C/T snv 6
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
rs121918080
TTR
0.827 0.240 18 31595128 missense variant G/A;T snv 2.4E-05 6
rs121918082
TTR
0.827 0.280 18 31595244 missense variant G/C snv 6
rs121918095
TTR
0.827 0.160 18 31598602 missense variant G/A snv 7.9E-04 2.2E-04 6
rs958191819
TTR
0.851 0.240 18 31595212 missense variant A/T snv 7.0E-06 6
rs2949506 0.851 0.160 18 30217168 intergenic variant C/T snv 0.14 5