Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs1047891 0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 28
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 26
rs646776 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs708272 0.708 0.440 16 56962376 intron variant G/A snv 0.42 0.38 24
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs629301 0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 22
rs1800961 0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 21
rs12229654 0.763 0.320 12 110976657 intergenic variant T/G snv 4.8E-03 20
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs261332 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs2266788 0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 19
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 19
rs174535 0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 19
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs1800775 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18