Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1799971 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs2234693 0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs9340799 0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs104893877 0.614 0.360 4 89828149 missense variant C/T snv 59
rs6280 0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs3918242 0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 54
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs324420 0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs1946518 0.602 0.760 11 112164735 intron variant T/G snv 0.60 46
rs1051730 0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 43
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs63751273 0.645 0.280 17 46010389 missense variant C/T snv 42
rs53576 0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs6295 0.645 0.200 5 63962738 intron variant C/G snv 0.49 40
rs16969968 0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 37
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36