Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs72653706 0.695 0.480 16 16163078 stop gained G/A snv 1.4E-03 1.2E-03 32
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs112735431 0.683 0.320 17 80385145 missense variant G/A;C snv 2.6E-04; 8.0E-06 24
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
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
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
rs80356814 0.732 0.320 1 156138697 synonymous variant C/T snv 8.0E-06 15
rs749437638 0.752 0.240 22 19968597 missense variant C/T snv 2.4E-05 1.4E-05 14
rs763000109
TNF
0.827 0.240 6 31575788 missense variant C/G;T snv 4.1E-06; 1.6E-05 9