Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3742330 0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 24
rs3135932 0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11 23
rs5743810 0.689 0.360 4 38828729 missense variant A/G snv 0.73 0.72 21
rs3819024 0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34 17
rs181206 0.742 0.440 16 28502082 missense variant A/G snv 0.28 0.24 16
rs4804803 0.732 0.360 19 7747847 upstream gene variant A/G snv 0.26 15
rs4135385 0.742 0.320 3 41237949 non coding transcript exon variant A/G snv 0.19 14
rs1131498 0.732 0.360 1 169707345 missense variant A/G snv 0.21 0.22 13
rs2060793 0.776 0.240 11 14893764 upstream gene variant A/G snv 0.63 11
rs3764880 0.752 0.320 X 12906707 start lost A/G snv 0.31 0.30 11
rs3811047 0.807 0.400 2 112913833 missense variant A/G snv 0.71 0.60 10
rs3093662
TNF
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 9
rs1061624 0.776 0.320 1 12207208 3 prime UTR variant A/G snv 0.48 8
rs4851527 0.790 0.160 2 102005914 intron variant A/G snv 0.63 7
rs754342091 0.790 0.200 9 117712421 missense variant A/G snv 3.2E-05 1.4E-05 7
rs10421768 0.807 0.120 19 35281996 intron variant A/G snv 0.21 6
rs2234711 0.827 0.080 6 137219383 5 prime UTR variant A/G snv 0.43 6
rs3917225 0.807 0.160 2 102152842 intron variant A/G snv 0.36 6
rs735239 0.851 0.240 19 7748382 upstream gene variant A/G snv 0.26 5
rs4842407 0.882 0.200 12 78807293 intron variant A/G snv 0.35 4
rs2280789 0.925 0.080 17 35879999 intron variant A/G snv 0.16 3
rs5743604 0.925 0.040 4 38799664 intron variant A/G snv 0.36 3
rs76600635 0.925 0.040 4 38798702 missense variant A/G snv 8.2E-03 2.8E-03 3
rs8105767 0.882 0.120 19 22032639 non coding transcript exon variant A/G snv 0.35 3
rs1135791 0.925 0.080 2 230177560 missense variant A/G snv 0.42 0.40 2