Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
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
rs2476601 0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs266729 0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs13266634 0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 23
rs2066808 0.807 0.280 12 56344189 intron variant A/G snv 0.21 8
rs11171806 0.807 0.360 12 56339747 synonymous variant G/A snv 4.9E-02 4.5E-02 7