Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs1169288 0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs651821 0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs17145738 0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11 11
rs2001945 8 125465736 upstream gene variant G/A;C;T snv 10
rs10808546 8 125483576 intron variant C/T snv 0.39 7
rs1168013 1.000 0.120 1 62531167 intron variant C/G;T snv 6
rs11206517 1.000 0.120 1 55060755 intron variant T/C;G snv 4