Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11111 0.882 0.080 5 37814000 3 prime UTR variant T/C snv 0.22 5
rs6903874 0.851 0.080 6 132575771 downstream gene variant T/C snv 0.23 5
rs9825823 0.851 0.080 3 61096480 intron variant T/C snv 0.47 5
rs772659997 0.882 0.120 10 49619853 synonymous variant T/C snv 2.0E-05 4
rs10997871 0.925 0.080 10 67913178 intron variant T/C snv 4.1E-03 3
rs2412646 0.882 0.120 4 55452605 3 prime UTR variant T/C snv 0.58 3
rs4658966 0.925 0.080 1 231942868 intron variant T/C snv 0.19 3
rs747052707 0.925 0.080 11 49192822 missense variant T/C snv 2.4E-05; 8.1E-06 3
rs9376026 0.925 0.080 6 134281316 intron variant T/C snv 0.43 3
rs7182853 1.000 0.040 15 66469947 intron variant T/C snv 0.31 1
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs11022778 0.925 0.080 11 13369313 intron variant T/A;G snv 6
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs1360780 0.708 0.320 6 35639794 intron variant T/A;C snv 31
rs2077647 0.732 0.320 6 151807942 synonymous variant T/A;C snv 8.1E-06; 0.46 16
rs9470080 0.827 0.080 6 35678658 intron variant T/A;C snv 13
rs1417938
CRP
0.776 0.320 1 159714396 intron variant T/A;C snv 0.28 10
rs28386840 0.827 0.080 16 55652906 upstream gene variant T/A;C snv 6
rs10848635 0.882 0.080 12 2207029 intron variant T/A;C snv 0.34 4
rs10997875 0.882 0.080 10 67920067 downstream gene variant T/A;C snv 4
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs553040076 0.925 0.080 19 10417700 missense variant T/A snv 4.5E-05 7.7E-05 3
rs797045032 0.827 0.280 7 143321720 missense variant GG/TC mnv 11
rs57875989 0.882 0.080 1 7829913 splice acceptor variant GCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGC/-;GCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGCGCTCTGTCCACAGGATCGCCTCCCATGAAGAATCCATCCCATCCTACTGCCAGC delins 0.11 0.18 7
rs1555206402 0.790 0.320 11 119093274 stop lost GCCCATTAACTGGTTTGTGGGGCACAGATGCCTGGGTTGCTGCTGTCCAGTGCCT/- delins 26