Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs780093 0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs11575937 0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs1801260 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs3135506 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs11542041 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 23
rs1042636 0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 23
rs2057482 0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs1169288 0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs8193036 0.689 0.600 6 52185695 upstream gene variant C/T snv 0.72 21
rs2074755 0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs651821 0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs2464196 0.742 0.320 12 120997624 missense variant G/A snv 0.34 0.27 17
rs3819024 0.701 0.560 6 52185988 upstream gene variant A/G snv 0.34 17
rs1800588 0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs118204057
LPL
0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 16
rs2075291 0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 15
rs773641005 0.742 0.240 16 58723829 missense variant T/C snv 14
rs1801177
LPL
0.742 0.240 8 19948197 missense variant G/A;C snv 1.4E-02; 2.0E-05 14
rs3812316 0.763 0.240 7 73606007 missense variant C/G snv 0.10 9.4E-02 14
rs4580704 0.790 0.200 4 55460540 intron variant G/C snv 0.69 13
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 12
rs11932595 0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs1337503417 0.790 0.160 17 41612325 missense variant G/T snv 4.0E-06 12