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
rs780094 0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1042713 0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1799983 0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246