Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800566 0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs121434592 0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs17879961 0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs121913273 0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs1138272 0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs401681 0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs833061 0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs2274223 0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs1800625 0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs752742313 0.637 0.320 3 138655502 missense variant C/T snv 1.2E-05 36
rs920778 0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs217727 0.641 0.480 11 1995678 non coding transcript exon variant G/A snv 0.20 34
rs886039484 0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs1801270 0.689 0.400 6 36684194 missense variant C/A;T snv 0.15; 4.4E-05 22
rs187115 0.695 0.320 11 35154612 intron variant T/C snv 0.37 22
rs2031920 0.695 0.240 10 133526341 non coding transcript exon variant C/T snv 3.1E-02 20
rs1047840 0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs735482 0.742 0.160 19 45408744 missense variant A/C snv 0.21 0.20 16
rs751402 0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15