Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs16933090 0.790 0.160 11 16434247 5 prime UTR variant C/T snv 0.12 7
rs17611
C5
0.732 0.480 9 121006922 missense variant C/T snv 0.47 0.36 14
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs20551 0.752 0.320 22 41152004 missense variant A/G snv 0.31 0.23 10
rs2066714 0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13
rs2075291 0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 15
rs2228315 0.807 0.120 12 108624122 missense variant C/T snv 0.11 0.14 7
rs2229116 0.827 0.080 15 33613209 missense variant A/G snv 0.23 0.21 9
rs2277680 0.776 0.160 17 4735268 missense variant G/A snv 0.47 0.41 10
rs2295490 0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4754 0.752 0.360 4 87981540 missense variant T/A;C snv 0.32 12
rs4925 0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28