Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs6921438 0.776 0.360 6 43957870 intergenic variant G/A;C snv 10
rs1740073 1.000 0.040 6 43979661 regulatory region variant T/C snv 0.67 2
rs2375981 1.000 0.040 9 2692583 regulatory region variant C/G;T snv 2
rs872129 0.925 0.080 1 203200263 intergenic variant A/G snv 0.19 2
rs1239681664
ABCA1
0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13
rs2066718
ABCA1
0.882 0.120 9 104826974 missense variant C/G;T snv 4.3E-04; 5.4E-02 7
rs2230808
ABCA1
0.827 0.240 9 104800523 missense variant T/C snv 0.71 0.60 6
rs138880920
ABCA1
1.000 0.040 9 104826957 missense variant C/G snv 3.3E-03 1.8E-03 1
rs33918808
ABCA1
1.000 0.040 9 104817351 missense variant C/G;T snv 3.5E-02; 4.0E-06 1
rs4147929
ABCA7
0.882 0.120 19 1063444 intron variant A/C;G snv 3
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs72653706
ABCC6
0.695 0.480 16 16163078 stop gained G/A snv 1.4E-03 1.2E-03 32
rs750249283
ABCG1
0.925 0.080 21 42296256 missense variant C/G;T snv 4.0E-06; 8.0E-06 2
rs1800888
ADRB2
0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs567798234
AMPD2
0.851 0.120 1 109625326 missense variant C/T snv 4.1E-06 7.0E-06 5
rs5742904
APOB
0.689 0.280 2 21006288 missense variant C/A;T snv 2.8E-04 7.3E-04 22
rs12713559
APOB
0.776 0.120 2 21006196 missense variant G/A snv 3.4E-04 5.0E-04 10
rs12817819
ATP2B1
0.882 0.040 12 89645549 intron variant C/T snv 9.4E-02 3
rs2293489
BUD23
0.925 0.120 7 73692949 non coding transcript exon variant C/T snv 0.26 2