Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs9349379 0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs200960801 0.827 0.200 6 151944488 missense variant A/G snv 4.0E-06 6
rs2523608 0.925 0.040 6 31354782 non coding transcript exon variant G/A snv 0.19 6
rs4713518 0.925 0.160 6 32289560 intron variant A/G;T snv 3
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs2854744 0.695 0.520 7 45921476 intron variant G/T snv 0.48 20
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 15
rs1251035592 1.000 0.040 7 99664039 missense variant T/C snv 4.2E-06 1
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs13281615 0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs1341991169
LPL
1.000 0.040 8 19939444 missense variant G/A snv 1
rs2230806 0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs2066714 0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13
rs2811712 0.882 0.080 9 21998036 intron variant G/A snv 0.85 5
rs717620 0.763 0.240 10 99782821 5 prime UTR variant C/T snv 0.17 0.15 10
rs10748835 0.827 0.160 10 102900499 non coding transcript exon variant G/A snv 0.41 5
rs174547 0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs174537 0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 23
rs694539 0.776 0.200 11 114262697 intron variant C/T snv 0.21 10
rs4757268 0.827 0.120 11 14789216 synonymous variant A/G snv 0.63 0.64 6
rs1941404 0.882 0.120 11 114298316 non coding transcript exon variant A/G snv 0.59 3