Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1294410 6 6738519 intron variant T/C snv 0.65 1
rs1294421 1.000 0.040 6 6742916 upstream gene variant T/A;C;G snv 1
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 3
rs13389219 1.000 0.080 2 164672366 intron variant C/T snv 0.47 5
rs1406948 20 35317816 intron variant G/A snv 0.44 1
rs143384 0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 1
rs1443512 12 53948900 downstream gene variant A/C;T snv 1
rs1457489 1.000 0.080 18 60194728 upstream gene variant G/A snv 0.29 2
rs15285
LPL
1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 1
rs17109256 14 79473650 intron variant G/A snv 0.21 1
rs17213965 16 15788110 intron variant C/T snv 0.24 1
rs17249754 0.882 0.120 12 89666809 intron variant G/A snv 0.15 3
rs17568628 5 76751114 intergenic variant T/C;G snv 1
rs1800437 0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 1
rs1876829 1.000 0.040 17 45834077 intron variant T/C snv 0.15 0.14 2
rs1883025 0.807 0.120 9 104902020 intron variant C/T snv 0.28 7
rs1993709 1.000 0.080 1 72372846 intron variant A/G snv 0.85 1
rs2074356 0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 12
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs2076529 1.000 0.120 6 32396178 synonymous variant T/C snv 0.41 0.39 2
rs2112347 0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 3
rs2119690 8 20002028 intergenic variant G/A;C snv 1
rs2145272 20 6645571 intergenic variant G/A;T snv 1
rs2229616 0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 2