Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs730881163
TTR
0.882 0.160 18 31595155 missense variant C/A snv 3
rs121918084
TTR
0.925 0.120 18 31595191 missense variant T/C snv 2
rs121918089
TTR
1.000 0.120 18 31598610 missense variant A/G snv 2
rs72922940
TTR
0.925 0.160 18 31590735 intron variant A/G snv 9.8E-02 2
rs730881167
TTR
0.925 0.120 18 31598638 missense variant A/C snv 2
rs730881169
TTR
0.925 0.120 18 31593020 missense variant C/A;T snv 2
rs11541790
TTR
1.000 0.120 18 31592956 missense variant C/T snv 7.0E-06 1
rs121918072
TTR
1.000 0.120 18 31595230 missense variant T/G snv 1
rs121918078
TTR
1.000 0.120 18 31593019 missense variant G/A snv 1
rs121918083
TTR
1.000 0.120 18 31592914 missense variant T/C snv 7.0E-06 1
rs121918096
TTR
1.000 0.120 18 31598652 inframe deletion GTC/- delins 1
rs1456101911
TTR
1.000 0.120 18 31598608 splice donor variant C/A;T snv 1