Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1039002 0.851 0.080 6 165741969 intron variant G/A;T snv 5
rs11789399 0.882 0.040 9 118597008 intergenic variant G/A;C snv 5
rs1344706 0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5
rs2054399 0.925 0.040 3 178623794 intron variant G/A;C snv 4
rs35753505 0.827 0.080 8 31616625 intergenic variant T/A;C snv 6
rs3730358 0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 14
rs3803300 0.827 0.120 14 104803442 3 prime UTR variant T/A;C snv 6
rs4765905 0.827 0.040 12 2240418 intron variant G/A;C snv 6
rs6994992 0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs778293 0.807 0.120 13 105516850 intergenic variant C/A;T snv 7
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801028 0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs17746001 0.925 0.040 4 179734472 intergenic variant C/T snv 5.3E-02 4
rs10994359 0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 7
rs886424 0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 10
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs802568 0.925 0.040 7 146262151 intron variant T/G snv 0.17 4
rs2524005 0.882 0.160 6 29931900 upstream gene variant G/A snv 0.18 5
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs6484218 0.882 0.040 11 10369034 intron variant G/A snv 0.21 5
rs12201676 0.925 0.040 6 89022382 regulatory region variant T/C snv 0.21 4
rs7872515 0.925 0.040 9 92060258 intron variant G/A snv 0.25 4