Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3025058 0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs3761581 0.851 0.160 X 129655744 upstream gene variant A/C snv 0.11 5
rs3087459 0.925 0.160 6 12289406 upstream gene variant A/C snv 0.20 2
rs2768759 0.851 0.200 1 156882671 downstream gene variant A/C;G snv 4
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs1801252 0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17
rs3850641 0.716 0.400 1 173206693 intron variant A/G snv 0.14 17
rs7528419 0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 13
rs5065 0.763 0.240 1 11846011 stop lost A/G snv 0.14 0.21 12
rs1265538677 0.790 0.200 13 46055808 synonymous variant A/G snv 4.0E-06 10
rs41507953 0.790 0.280 8 27500988 missense variant A/G snv 8.7E-02 0.13 10
rs1801222 0.925 0.160 10 17114152 missense variant A/G snv 0.73 0.72 5
rs5070 0.882 0.160 11 116837304 intron variant A/G snv 0.56 0.60 5
rs1187513719 0.851 0.200 10 94780595 missense variant A/G snv 4.0E-06 4
rs10757279 0.925 0.040 9 22124631 intron variant A/G snv 0.40 3
rs181937009 0.925 0.040 6 140064258 intron variant A/G snv 0.23 3
rs1967309 0.925 0.080 16 4015582 non coding transcript exon variant A/G snv 0.51 3
rs2235312 0.882 0.160 X 129653118 intron variant A/G snv 0.31 3
rs12766939 0.925 0.160 10 17031136 intron variant A/G snv 0.23 2
rs144972973 0.925 0.040 15 44272494 intergenic variant A/G snv 1.8E-02 2