Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72613567 0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs9891119 0.882 0.120 17 42355962 intron variant A/C snv 0.36 3
rs6843722 1.000 0.040 4 55465165 intron variant A/C snv 0.30 1
rs1044498 0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs2645424 0.827 0.120 8 11826954 intron variant A/C;G snv 0.56 5
rs4686434 1.000 0.040 3 186647354 intron variant A/C;G snv 1
rs5764455 1.000 0.040 22 44002644 intron variant A/C;G snv 1
rs854560 0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs1131580 0.882 0.160 3 172505830 3 prime UTR variant A/C;G;T snv 4
rs698718 1.000 0.040 16 68526282 upstream gene variant A/C;G;T snv 1
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs1137100 0.627 0.640 1 65570758 missense variant A/G snv 0.30 0.25 39
rs12980275 0.701 0.360 19 39241143 upstream gene variant A/G snv 0.36 23
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 16
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs2241767 0.763 0.440 3 186853407 intron variant A/G snv 0.10 10
rs3774261 0.776 0.320 3 186853770 splice region variant A/G snv 0.55 10
rs4374383 0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10