Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 70
rs76992529
TTR
0.653 0.560 18 31598655 missense variant G/A snv 1.1E-03 4.9E-03 36
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs1800730 0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs225014 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 22
rs8193036 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs12212067 0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs1568523935 0.776 0.240 19 19105656 stop gained C/G snv 20
rs267607161
TTR
0.742 0.360 18 31598580 missense variant G/T snv 4.0E-06 7.0E-06 16
rs45546039 0.732 0.120 3 38613781 missense variant C/A;T snv 4.1E-06 15
rs104894201 0.763 0.280 11 111908934 missense variant T/C snv 12
rs121908987 0.742 0.200 7 151576412 missense variant C/A;G;T snv 4.0E-06 12
rs138119149 0.807 0.280 6 44304512 missense variant G/A snv 2.1E-04 2.4E-04 11
rs121918312 0.776 0.160 10 119672373 missense variant C/A;T snv 11
rs766265889 0.827 0.240 2 178535508 stop gained G/A;T snv 8.0E-06; 4.0E-06 11
rs121918100
TTR
0.827 0.160 18 31595184 missense variant T/C snv 11
rs58034145 0.827 0.160 1 156134830 missense variant A/C snv 10
rs114638163 0.827 0.240 13 23805994 stop gained C/A;T snv 4.0E-06; 1.3E-03 10