Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1063192 0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 24
rs10738610 0.882 0.120 9 22123767 intron variant A/C;T snv 5
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
rs10978777 1.000 0.080 9 107268309 intergenic variant G/A;C snv 2
rs113533135 1.000 0.080 2 140268867 intron variant T/C snv 2.0E-02 2
rs113805659 1.000 0.080 7 78663475 intron variant G/C snv 6.1E-02 2
rs114031744 1.000 0.080 10 123610085 intergenic variant A/G snv 1.7E-02 2
rs11509197 1.000 0.080 7 118641356 intergenic variant C/T snv 0.38 2
rs115689251 1.000 0.080 17 36032377 intergenic variant A/C snv 1.0E-02 2
rs117854110 1.000 0.080 7 105603002 upstream gene variant C/A;T snv 2
rs12040333 1.000 0.080 1 43848369 intron variant G/A;C snv 2
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs13175840 1.000 0.080 5 133861647 regulatory region variant A/G snv 0.25 2
rs1333045 0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 14
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1412829 0.742 0.400 9 22043927 intron variant A/G snv 0.28 14
rs1440581 1.000 0.080 4 88305270 intron variant T/A;C snv 4
rs1481805 1.000 0.080 8 71121190 intron variant A/T snv 0.58 2
rs1532002 1.000 0.080 2 140292500 intron variant G/A snv 2.3E-02 2
rs16879003 1.000 0.080 6 16745008 intron variant T/C;G snv 2
rs17214144 1.000 0.080 7 24846128 intron variant T/C snv 0.20 2
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs2680830 1.000 0.080 2 17596817 intron variant A/G;T snv 0.94 2