Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs16933090 0.790 0.160 11 16434247 5 prime UTR variant C/T snv 0.12 7
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs7439293 0.807 0.080 4 168756335 non coding transcript exon variant G/A snv 0.44 6
rs74577862 0.882 0.080 3 186843903 intron variant G/A snv 1.8E-02 3
rs877087 0.882 0.080 15 33582074 intron variant T/C;G snv 4
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs879254850 0.776 0.160 19 11113365 missense variant A/G;T snv 4.0E-06 9
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs2295490 0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs2075291 0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 15
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs5355 0.742 0.240 1 169726729 missense variant G/A snv 4.5E-02 3.3E-02 14
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs2228315 0.807 0.120 12 108624122 missense variant C/T snv 0.11 0.14 7
rs1799864 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 68
rs3732378 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs2066714 0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs2229116 0.827 0.080 15 33613209 missense variant A/G snv 0.23 0.21 9
rs4925 0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28