Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 27
rs1013940 0.827 0.160 2 107992192 missense variant A/G snv 9.3E-02 7.4E-02 6
rs10223646
DSE
0.882 0.080 6 116296236 intron variant C/T snv 0.41 4
rs1033656351 0.827 0.160 12 121232997 missense variant G/A snv 1.6E-05 2.8E-05 7
rs10410544 0.827 0.120 19 38894892 intron variant T/C snv 0.68 0.67 6
rs1042173 0.763 0.320 17 30197993 3 prime UTR variant A/C snv 0.40 14
rs1043307 0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs10434 0.701 0.480 6 43785475 3 prime UTR variant A/G snv 0.59 17
rs1044396 0.742 0.240 20 63349782 missense variant G/A;C snv 0.47; 6.1E-05 17
rs1044397 0.851 0.160 20 63349752 synonymous variant C/T snv 0.48 0.41 7
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs10510057 0.925 0.080 10 119551536 intergenic variant G/C snv 0.22 3
rs10514299 0.827 0.120 5 88367793 intron variant C/T snv 0.21 6
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs1061622 0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs10766075 0.925 0.080 11 13297040 intron variant C/T snv 0.27 6
rs1082214
MIP
0.925 0.080 12 56452706 non coding transcript exon variant C/T snv 9.3E-02 6
rs10830963 0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs10848635 0.882 0.080 12 2207029 intron variant T/A;C snv 0.34 4
rs10988134 0.925 0.080 9 128833128 3 prime UTR variant C/T snv 0.34 4
rs10997871 0.925 0.080 10 67913178 intron variant T/C snv 4.1E-03 3
rs10997875 0.882 0.080 10 67920067 downstream gene variant T/A;C snv 4
rs11022778 0.925 0.080 11 13369313 intron variant T/A;G snv 6
rs11030101 0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36 10