Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
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
rs121918098
TTR
0.807 0.200 18 31592939 missense variant A/G snv 7
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
rs958191819
TTR
0.851 0.240 18 31595212 missense variant A/T snv 7.0E-06 6
rs104894665
TTR
0.851 0.120 18 31593017 missense variant T/C snv 5
rs121918071
TTR
0.882 0.240 18 31595209 missense variant C/A snv 4
rs1555631390
TTR
0.851 0.160 18 31595128 inframe insertion -/AGTCTG delins 4
rs121918069
TTR
0.925 0.200 18 31595152 missense variant T/A;G snv 3
rs121918073
TTR
0.882 0.160 18 31598622 missense variant C/A snv 3
rs121918076
TTR
0.882 0.120 18 31595129 missense variant T/A;C;G snv 3
rs121918077
TTR
0.882 0.120 18 31592992 missense variant G/C snv 3
rs121918081
TTR
0.925 0.200 18 31595124 missense variant A/G snv 3
rs121918086
TTR
1.000 0.120 18 31595160 missense variant G/A snv 3
rs121918087
TTR
0.882 0.120 18 31598581 missense variant C/G snv 3
rs386134269
TTR
0.882 0.120 18 31595127 missense variant A/C;G snv 3
rs387906523
TTR
0.882 0.160 18 31593025 missense variant G/A;C snv 3