Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs605066 6 139508529 intron variant C/T snv 0.53 6
rs645040 3 136207780 upstream gene variant G/T snv 0.77 6
rs718314 0.882 0.120 12 26300350 intron variant A/G snv 0.27 6
rs15285
LPL
1.000 0.040 8 19967156 3 prime UTR variant C/T snv 0.36 5
rs2845885 11 64101590 intron variant C/T snv 0.87 5
rs634869 6 139510620 intron variant T/A;C snv 5
rs72959041 6 127133748 intron variant G/A snv 3.2E-02 5
rs9991328 4 88791970 intron variant C/T snv 0.53 5
rs1011731 1 172377408 intron variant G/A snv 0.46 4
rs2207132 20 40513876 intergenic variant G/A snv 2.7E-02 4
rs78058190 2 218835276 upstream gene variant G/A snv 3.9E-02 4
rs900399 3 157080943 upstream gene variant A/G snv 0.36 4
rs4660808 1 39552837 intron variant C/T snv 0.17 3
rs4738141 8 71557507 intron variant A/G snv 0.41 3
rs10101067 8 71495139 intron variant G/C snv 6.2E-02 2
rs3851294 1 205161285 missense variant A/G;T snv 0.93 2
rs56271783 11 64237251 intron variant G/A;C;T snv 3.6E-05; 3.7E-02 2
rs797486 13 50647482 intron variant C/A snv 0.85 2