Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10754558 0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10811656 0.807 0.200 9 22124473 intron variant C/T snv 0.47 7
rs12190287 0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 19
rs1239681664 0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1799750 0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1799964 0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 47
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 15
rs28362491 0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs3025058 0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs3850641 0.716 0.400 1 173206693 intron variant A/G snv 0.14 17
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs6922269 0.807 0.200 6 150931849 intron variant G/A snv 0.35 7
rs8075977 0.827 0.160 17 1757507 upstream gene variant T/C snv 0.37 5
rs8259
BSG
0.776 0.200 19 582927 3 prime UTR variant T/A snv 0.39 9
rs9818870 0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv 9
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2259816 0.827 0.280 12 120997784 synonymous variant G/A;T snv 6.7E-06; 0.40 8