Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1058046
PYY
0.925 0.120 17 43953163 missense variant G/C snv 0.63 0.59 2
rs10885406 0.925 0.120 10 113017965 intron variant A/G snv 0.55 2
rs11076023
FTO
0.925 0.120 16 54118136 3 prime UTR variant A/T snv 0.49 2
rs11960429 0.925 0.120 5 180739677 missense variant G/A snv 1.2E-02 1.5E-02 2
rs12156368 0.925 0.120 8 18885203 intron variant C/T snv 0.36 2
rs1541276 0.925 0.120 18 13825728 splice region variant A/C snv 0.17 0.19 2
rs1550805 0.925 0.120 5 68287979 intron variant C/T snv 6.9E-02 2
rs16861194 0.925 0.120 3 186841636 upstream gene variant A/G snv 0.15 2
rs1797 0.925 0.120 10 117945927 intergenic variant C/T snv 0.45 2
rs1926065 0.925 0.120 20 56256281 intergenic variant G/A snv 0.31 2
rs1968482 0.925 0.120 2 24863989 intron variant T/C snv 0.32 2
rs200027152 0.925 0.120 11 73975612 missense variant C/T snv 8.0E-05 4.9E-05 2
rs201777403 0.925 0.120 5 148827105 missense variant G/A snv 4.0E-06 2
rs2028299 0.925 0.120 15 89831025 3 prime UTR variant C/A snv 0.72 2
rs2118404 0.925 0.120 2 25154460 3 prime UTR variant C/A;G;T snv 2
rs225011 0.925 0.120 14 80205865 intron variant T/A;C snv 2
rs2302870 0.925 0.120 2 207088682 intron variant T/C;G snv 2
rs3746876 0.925 0.120 21 38299525 synonymous variant C/T snv 2.0E-02 3.2E-02 2
rs4325426 0.925 0.120 13 40642300 intron variant C/A snv 0.41 2
rs4450508 0.925 0.120 18 60246201 intergenic variant G/A snv 0.31 2
rs6064099 0.925 0.120 20 54643425 intron variant G/C snv 0.30 0.36 2
rs6983992 0.925 0.120 8 18871125 intron variant T/C snv 0.20 2
rs706713 0.925 0.120 5 68226894 synonymous variant C/T snv 0.31 0.31 2
rs708277
FTO
0.925 0.120 16 54114023 3 prime UTR variant G/A snv 0.62 2
rs7181866 0.925 0.120 15 50318595 intron variant A/G snv 6.6E-02 2