Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1428103360 1.000 0.040 5 70070732 missense variant A/G snv 2
rs143061887 0.925 0.080 1 226881960 missense variant C/T snv 1.6E-05 5.6E-05 3
rs143624519 0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17
rs1481950 1.000 0.080 8 53777725 intron variant C/A;G snv 2
rs149215094 1.000 0.080 20 58444203 missense variant G/A snv 5.6E-05 5.6E-05 2
rs156697 0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 25
rs17125721 0.763 0.120 14 73206470 missense variant A/G snv 1.5E-02 1.5E-02 14
rs1799945 0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1799990 0.683 0.440 20 4699605 missense variant A/G snv 0.31 0.33 23
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1990622 0.742 0.200 7 12244161 downstream gene variant A/G snv 0.52 16
rs200161705 0.882 0.160 4 169585374 missense variant C/A;T snv 6.0E-05; 2.3E-03 5
rs2275294 0.925 0.080 20 63962894 intron variant G/A snv 0.25 3
rs2435200 0.925 0.080 17 45994485 intron variant G/A snv 0.40 5
rs2435211 17 45985878 intron variant C/G;T snv 1
rs267606900 1.000 10 30313926 missense variant T/C snv 1.4E-05 2
rs28933979
TTR
0.587 0.600 18 31592974 missense variant G/A;C snv 1.0E-04 70
rs3173615 0.807 0.200 7 12229791 missense variant C/A;G snv 0.49 12
rs34015634 0.851 0.120 12 40340380 missense variant T/C snv 3.2E-05 1.4E-05 8
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs35801418 0.827 0.120 12 40321114 missense variant A/G snv 7
rs371557337 1.000 0.040 5 150733475 start lost T/C;G snv 7.0E-06 2
rs3857059 1.000 0.040 4 89754087 intron variant A/G;T snv 2
rs387907043 0.925 0.120 20 63930873 missense variant T/A;G snv 4.0E-06 3
rs397515634 0.925 0.040 4 41256996 missense variant A/C snv 4.0E-06 3