Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4823006 22 29055683 3 prime UTR variant A/G snv 0.41 1
rs1406948 20 35317816 intron variant G/A snv 0.44 1
rs143384 0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 1
rs2145272 20 6645571 intergenic variant G/A;T snv 1
rs2075650 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs4420638 0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs2278426 1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 2
rs2287019 1.000 0.080 19 45698914 intron variant C/T snv 0.17 0.16 2
rs1800437 0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 1
rs3786897 1.000 0.080 19 33402102 intron variant A/G snv 0.45 1
rs7246865 19 17108295 intron variant G/A snv 0.36 1
rs6567160 1.000 0.080 18 60161902 upstream gene variant T/C snv 0.21 3
rs1457489 1.000 0.080 18 60194728 upstream gene variant G/A snv 0.29 2
rs2229616 0.732 0.200 18 60372043 missense variant C/T snv 1.6E-02 1.6E-02 2
rs12454712 0.925 0.120 18 63178651 intron variant T/A;C snv 1
rs8070723 0.851 0.240 17 46003698 intron variant A/G snv 0.18 5
rs12936587 0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38 3
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 3
rs1876829 1.000 0.040 17 45834077 intron variant T/C snv 0.15 0.14 2
rs4640244 17 21380911 intron variant A/G snv 0.33 1
rs757608 17 61419916 regulatory region variant A/G;T snv 1
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 9
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 6
rs7498665 0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 5