Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs313158 6 85334045 intergenic variant A/T snv 1.8E-02 1
rs2144151 20 903001 intron variant T/G snv 0.40 1
rs764821003 3 30671823 missense variant G/A snv 1.4E-05 1
rs34203073 1.000 0.040 5 77035624 missense variant G/A snv 1.0E-02 9.9E-03 2
rs759985000 11 27700987 5 prime UTR variant G/A;C snv 4.2E-06; 8.4E-06 2
rs6809699 1.000 0.080 3 151338810 synonymous variant A/C snv 0.87 0.88 2
rs1967309 0.925 0.080 16 4015582 non coding transcript exon variant A/G snv 0.51 3
rs387906853 0.925 0.040 15 67181297 stop gained G/A;T snv 3
rs755460305 0.882 0.080 3 186732650 missense variant C/A snv 4
rs12938 0.851 0.160 1 169691640 3 prime UTR variant A/G snv 0.27 5
rs267606743 1.000 0.160 13 110192222 missense variant C/T snv 5
rs1800458
TTR
0.851 0.280 18 31592902 missense variant G/A snv 5.1E-02 5.2E-02 5
rs121918095
TTR
0.827 0.160 18 31598602 missense variant G/A snv 7.9E-04 2.2E-04 6
rs121918027
PLG
0.827 0.320 6 160738593 missense variant G/A snv 1.4E-03 3.5E-04 7
rs28933981
TTR
0.807 0.200 18 31598647 missense variant C/T snv 1.5E-03 1.7E-03 8
rs763000109
TNF
0.827 0.240 6 31575788 missense variant C/G;T snv 4.1E-06; 1.6E-05 9
rs749437638 0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05 14
rs80356814 0.732 0.320 1 156138697 synonymous variant C/T snv 8.0E-06 15
rs1122608 0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs1042579 0.732 0.240 20 23048087 missense variant G/A;T snv 0.19 16
rs505151 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 18
rs765798193 0.732 0.320 12 121915884 frameshift variant G/-;GG delins 18
rs2303790 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 19
rs14259 0.724 0.360 12 121915890 missense variant A/C;G snv 4.0E-06; 0.32 19
rs112735431 0.683 0.320 17 80385145 missense variant G/A;C snv 2.6E-04; 8.0E-06 24