Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9904341 0.695 0.280 17 78214286 5 prime UTR variant G/A;C;T snv 0.38; 4.8E-06 20
rs778574118 1.000 0.040 10 113721138 missense variant A/G snv 4.0E-06 1
rs1052571 0.882 0.080 1 15524118 missense variant G/A snv 0.50 0.59 4
rs1132312 1.000 0.040 1 15518120 missense variant A/C;G;T snv 0.53 1
rs78655421 0.716 0.240 7 117530975 missense variant G/A;C;T snv 1.5E-03; 1.2E-05 18
rs213950 0.716 0.320 7 117559479 missense variant G/A snv 0.47 0.57 16
rs777418530 0.763 0.120 16 84845883 missense variant A/G snv 4.0E-06 7.0E-06 10
rs497078 0.925 0.040 1 15440540 synonymous variant C/A;T snv 3.7E-03; 9.1E-02 2
rs4073 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 64
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs2071746 0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs16944 0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs1143634 0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 52
rs4251961 0.763 0.200 2 113116890 intron variant T/C snv 0.29 10
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800796 0.555 0.760 7 22726627 non coding transcript exon variant G/C snv 9.9E-02 74
rs1451659304 1.000 0.040 16 868990 missense variant A/C snv 2
rs371282890
LPL
0.827 0.120 8 19955900 missense variant C/G snv 1.1E-04 6.3E-05 6
rs773891125
LPL
0.827 0.120 8 19955896 frameshift variant CT/- delins 6
rs145657341
LPL
0.925 0.120 8 19951811 missense variant G/A snv 1.7E-04 7.0E-05 3
rs12688220 0.827 0.200 X 107001537 upstream gene variant C/T snv 0.19 5