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
rs10275045 0.882 0.160 7 1881190 intron variant C/T snv 0.35 5
rs1039002 0.851 0.080 6 165741969 intron variant G/A;T snv 5
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs10994359 0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 7
rs1130214 0.742 0.280 14 104793397 5 prime UTR variant C/A snv 0.31 12
rs11789399 0.882 0.040 9 118597008 intergenic variant G/A;C snv 5
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12201676 0.925 0.040 6 89022382 regulatory region variant T/C snv 0.21 4
rs12966547 0.827 0.040 18 55084786 intergenic variant G/A snv 0.39 7
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs135745 0.763 0.200 22 38287631 downstream gene variant G/C snv 0.48 13
rs1625579 0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs165599 0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5
rs17746001 0.925 0.040 4 179734472 intergenic variant C/T snv 5.3E-02 4
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs1801028 0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs2054399 0.925 0.040 3 178623794 intron variant G/A;C snv 4
rs2239547 0.882 0.040 3 52821213 intron variant T/C snv 0.27 6
rs2251219 0.732 0.120 3 52550771 synonymous variant T/C;G snv 0.39; 4.0E-06 0.34 14
rs2391191 0.807 0.080 13 105467097 missense variant G/A snv 0.40 0.32 7
rs2524005 0.882 0.160 6 29931900 upstream gene variant G/A snv 0.18 5
rs35753505 0.827 0.080 8 31616625 intergenic variant T/A;C snv 6