Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs237025 0.672 0.360 6 149400554 missense variant G/A snv 0.55 0.57 26
rs660339 0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs759853 0.827 0.320 7 134459206 non coding transcript exon variant G/A snv 0.33 6
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs1501299 0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs16139 0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs713041 0.776 0.400 19 1106616 stop gained T/A;C snv 4.2E-06; 0.58 16
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
rs1549758 0.807 0.360 7 150998638 synonymous variant T/C snv 0.76 0.76 7
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs2241766 0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306