Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs3184504 0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
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
rs351855 0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 58
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
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs653178 0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs855791 0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 38
rs28929474 0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs405509 0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs11887534 0.653 0.440 2 43839108 missense variant G/A;C snv 6.4E-06; 6.7E-02 29
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs646776 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25