Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7452939 0.882 0.080 6 132572626 downstream gene variant G/A snv 4
rs143830698
ACE
0.882 0.120 17 63488659 missense variant G/A snv 8.4E-05 4
rs769397961
ACE
0.882 0.120 17 63488758 missense variant G/A snv 1.2E-05 3.5E-05 4
rs1863918 0.882 0.160 5 179112381 3 prime UTR variant G/T snv 0.25 4
rs2228079 0.882 0.160 1 203129147 synonymous variant T/G snv 0.31 0.26 4
rs1800035 0.925 0.080 10 111078794 missense variant C/G;T snv 1.9E-03 4
rs10848635 0.882 0.080 12 2207029 intron variant T/A;C snv 0.34 4
rs772659997 0.882 0.120 10 49619853 synonymous variant T/C snv 2.0E-05 4
rs11636753 0.882 0.120 15 78636604 intron variant G/T snv 0.35 4
rs10223646
DSE
0.882 0.080 6 116296236 intron variant C/T snv 0.41 4
rs760761 0.882 0.080 6 15650901 intron variant G/A snv 0.26 4
rs4672619 0.882 0.160 2 211592470 intron variant C/A;G snv 4
rs2910709 0.882 0.120 5 37811762 non coding transcript exon variant A/G;T snv 4
rs561077 0.882 0.080 X 151181177 missense variant A/G snv 0.43 0.45 4
rs1800041 0.882 0.120 5 63961673 missense variant G/A snv 1.8E-03 5.3E-04 4
rs3125 0.925 0.080 13 46834716 3 prime UTR variant C/G;T snv 4
rs10988134 0.925 0.080 9 128833128 3 prime UTR variant C/T snv 0.34 4
rs4792887 0.882 0.080 17 45799654 non coding transcript exon variant C/T snv 0.16 4
rs1858232 0.882 0.080 1 162334048 intron variant A/G;T snv 4
rs386231 0.882 0.080 1 162356033 intron variant C/T snv 0.68 4
rs1402757753 0.882 0.080 12 132621913 missense variant G/A snv 7.0E-06 4
rs755302767 0.882 0.080 12 132621835 missense variant G/A snv 4.0E-06 4
rs371356064 0.882 0.120 12 121133072 synonymous variant C/T snv 1.2E-05 7.0E-06 4
rs17759843 0.882 0.080 22 21920372 3 prime UTR variant G/A snv 6.7E-02 4
rs115482041 0.925 0.080 9 4860267 missense variant C/T snv 2.6E-03 2.3E-03 4