Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs1232898090 0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36
rs17782313 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 34
rs8192678 0.667 0.440 4 23814039 missense variant C/T snv 0.31 0.26 28
rs12970134 0.790 0.280 18 60217517 intergenic variant G/A snv 0.21 13
rs2920502 0.851 0.160 3 12287696 intron variant G/C snv 0.27 6