Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs6313 0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs6296 0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs5569 0.742 0.280 16 55697923 synonymous variant G/A;C snv 0.31; 4.0E-06 19
rs3746544 0.790 0.120 20 10306436 3 prime UTR variant G/T snv 0.68 10
rs3745406 0.851 0.080 19 53891711 missense variant T/A;C snv 4.0E-06; 0.41 6
rs6191 0.925 0.040 5 143278591 3 prime UTR variant C/A snv 0.48 4