Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11591147 0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 4
rs505151 0.732 0.360 1 55063514 missense variant G/A snv 0.95 0.90 3
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs102275 0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 6
rs174583 0.807 0.320 11 61842278 intron variant C/T snv 0.35 5
rs3780181 1.000 0.320 9 2640759 intron variant A/G snv 0.11 3
rs2464196 0.742 0.320 12 120997624 missense variant G/A snv 0.34 0.27 2
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 12
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 11
rs174535 0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 8
rs3846662 0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 5
rs4506565 0.790 0.280 10 112996282 intron variant A/G;T snv 4
rs1333045 0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 3
rs2303790 0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 3
rs4148217 0.790 0.280 2 43872294 missense variant C/A;T snv 0.21; 1.2E-05 3
rs5742904 0.689 0.280 2 21006288 missense variant C/A;T snv 2.8E-04 7.3E-04 3
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 2
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 13
rs17696736 0.827 0.240 12 112049014 intron variant A/G snv 0.30 11
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 10
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 10
rs646776 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs6857 0.790 0.240 19 44888997 3 prime UTR variant C/T snv 0.13 8
rs1042034 0.851 0.240 2 21002409 missense variant C/T snv 0.70 0.78 7