Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs5743708 0.525 0.800 4 153705165 missense variant G/A snv 1.7E-02 1.8E-02 98
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 43
rs2569190 0.620 0.560 5 140633331 intron variant A/G snv 0.57 39
rs57095329 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs4898 0.672 0.520 X 47585586 synonymous variant T/C snv 0.46 0.46 25
rs225014 0.695 0.400 14 80203237 missense variant T/C snv 0.41 0.39 22
rs1045411 0.708 0.360 13 30459095 3 prime UTR variant C/T snv 0.20 18
rs747126003 0.689 0.400 7 22728790 missense variant A/G;T snv 4.0E-06 18
rs653765 0.763 0.240 15 58749813 upstream gene variant T/C;G snv 0.45 10
rs2234237 0.763 0.280 6 41282728 missense variant T/A snv 0.13 0.12 9
rs1974226 0.827 0.240 6 52190537 3 prime UTR variant C/T snv 0.15 6
rs12692386 0.827 0.160 2 9555777 5 prime UTR variant A/G snv 0.72 5
rs6586282
CBS
0.882 0.080 21 43058387 intron variant C/T snv 5
rs2857656 0.851 0.120 17 34254988 upstream gene variant G/A;C snv 5
rs1475145065 0.882 0.080 14 24574706 missense variant C/G;T snv 4.0E-06; 8.0E-06 3
rs1361600 0.925 0.120 1 94542362 upstream gene variant C/T snv 0.51 3
rs10506481 0.882 0.080 12 66250331 3 prime UTR variant T/C snv 9.0E-02 3
rs773829498 0.882 0.080 7 101130457 missense variant A/G snv 4.0E-06 3