Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2071746 0.708 0.320 22 35380679 intron variant A/T snv 0.49 18
rs4251961 0.763 0.200 2 113116890 intron variant T/C snv 0.29 10
rs7057398 0.827 0.080 X 106901299 intron variant T/C snv 0.41 5
rs5029924 0.851 0.200 6 137866361 intron variant C/T snv 0.13 4
rs5707
REN
1.000 0.040 1 204160543 intron variant A/C;G;T snv 0.25; 2.0E-05; 1.2E-05 2
rs5743795 1.000 0.040 4 38830874 intron variant C/T snv 0.14 1
rs748405415 0.790 0.160 7 142773993 stop gained G/A;T snv 8
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs4986791 0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs11209026 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 46
rs17107315 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 40
rs76863441 0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03 25
rs1223231582 0.677 0.280 7 142750639 missense variant A/G snv 7.0E-06 24
rs121912654 0.683 0.400 17 7675143 missense variant C/A;T snv 4.0E-05 21
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
rs111033565 0.742 0.120 7 142751938 missense variant G/A snv 1.2E-05 11
rs111033566 0.742 0.280 7 142750600 missense variant A/C;T snv 11
rs267606982 0.742 0.120 7 142751938 missense variant GC/AT mnv 11
rs777418530 0.763 0.120 16 84845883 missense variant A/G snv 4.0E-06 7.0E-06 10
rs61734659 0.790 0.160 7 142774035 missense variant G/A snv 1.4E-02 8
rs371282890
LPL
0.827 0.120 8 19955900 missense variant C/G snv 1.1E-04 6.3E-05 6