Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs662 0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1801282 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs738409 0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1137101 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs11549465 0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs56149945 0.595 0.680 5 143399752 missense variant T/A;C snv 2.0E-02 49
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs1800797 0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs7799039 0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs11575937 0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs1801260 0.695 0.280 4 55435202 3 prime UTR variant A/G snv 0.25 28
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs4402960 0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs80356616 0.732 0.360 11 17387917 missense variant C/T snv 19