Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10196867 0.925 0.080 2 79751234 intron variant C/G;T snv 5
rs147247472 0.925 0.080 1 49441901 intron variant G/A snv 7.3E-04 5
rs2133896 0.925 0.080 12 99455122 intron variant G/T snv 7.6E-02 5
rs10198241 0.925 0.080 2 226115660 intergenic variant T/C snv 0.58 4
rs115357105 0.925 0.080 9 104376689 intergenic variant A/G snv 1.5E-02 4
rs11681792 1.000 0.080 2 49957256 intron variant C/T snv 0.12 4
rs11825659 0.925 0.080 11 133925624 intron variant A/G snv 0.12 4
rs12180309 0.925 0.080 6 91209048 intergenic variant C/T snv 1.9E-02 4
rs12544026 0.925 0.080 8 101819970 intron variant G/A snv 0.85 4
rs139438618 0.882 0.080 7 84008281 intron variant A/G snv 5.2E-02 4
rs17028615 1.000 0.080 4 99150767 intron variant A/C;G snv 4
rs1789882 1.000 0.080 4 99313896 synonymous variant A/G;T snv 0.82 4
rs2094081 0.925 0.080 1 38927359 intron variant G/A;C snv 4
rs3743832 1.000 0.080 16 9120023 3 prime UTR variant A/C snv 0.55 4
rs55702914 0.925 0.080 2 197349672 intergenic variant C/G snv 0.37 4
rs58598658 0.925 0.080 13 73887725 intron variant -/A;AA delins 4
rs72737330 0.925 0.080 1 216600151 intron variant T/C snv 0.15 4
rs79246196 0.925 0.080 7 100185286 intron variant C/T snv 1.8E-02 4
rs1000579 1.000 0.080 4 4717767 intron variant A/G snv 0.44 3
rs10211296 1.000 0.080 2 165633833 intron variant A/G snv 0.34 3
rs10483038 1.000 0.080 21 37652469 intron variant T/C snv 0.26 3
rs11075992
FTO
1.000 0.080 16 53786154 intron variant T/C snv 0.41 3
rs111372083 1.000 0.080 21 37638374 intron variant C/A;T snv 0.27 3
rs111576572 1.000 0.080 21 37617262 3 prime UTR variant A/G snv 0.32 3
rs1154433 1.000 0.080 4 99332551 intron variant A/G;T snv 3