Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 10
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 4
rs1555631390
TTR
0.851 0.160 18 31595128 inframe insertion -/AGTCTG delins 4
rs121918091
TTR
0.882 0.200 18 31595169 missense variant T/C snv 4.0E-06 3
rs121918070
TTR
1.000 0.120 18 31595157 missense variant A/G snv 4.0E-06 1.4E-05 2
rs79977247
TTR
0.776 0.200 18 31592975 missense variant T/C;G snv 2
rs121918098
TTR
0.807 0.200 18 31592939 missense variant A/G snv 2
rs121918100
TTR
0.827 0.160 18 31595184 missense variant T/C snv 2
rs104894665
TTR
0.851 0.120 18 31593017 missense variant T/C snv 2
rs121918072
TTR
1.000 0.120 18 31595230 missense variant T/G snv 1
rs1567945632
TTR
1.000 0.120 18 31592938 missense variant G/A snv 1
rs1555631387
TTR
1.000 0.120 18 31595125 missense variant C/G snv 1
rs121918083
TTR
1.000 0.120 18 31592914 missense variant T/C snv 7.0E-06 1
rs121918071
TTR
0.882 0.240 18 31595209 missense variant C/A snv 1
rs121918082
TTR
0.827 0.280 18 31595244 missense variant G/C snv 1
rs121918087
TTR
0.882 0.120 18 31598581 missense variant C/G snv 1
rs121918085
TTR
0.882 0.160 18 31595181 missense variant A/T snv 1.6E-05 3.5E-05 1
rs1555631402
TTR
1.000 0.120 18 31595163 missense variant G/A snv 1
rs386134269
TTR
0.882 0.120 18 31595127 missense variant A/C;G snv 1
rs121918094
TTR
0.827 0.280 18 31592921 missense variant T/C snv 1
rs267607161
TTR
0.742 0.360 18 31598580 missense variant G/T snv 4.0E-06 7.0E-06 1
rs876658108
TTR
1.000 0.120 18 31598649 missense variant G/T snv 1
rs121918080
TTR
0.827 0.240 18 31595128 missense variant G/A;T snv 2.4E-05 1
rs121918074
TTR
0.851 0.120 18 31595247 missense variant C/A snv 6.0E-04 3.9E-04 1
rs387906523
TTR
0.882 0.160 18 31593025 missense variant G/A;C snv 1