Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1800437 0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 13
rs1801253 0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs964184 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs1042714 0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs5370 0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62