Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2227631
SERPINE1
0.742 0.200 7 101126257 upstream gene variant A/G snv 0.54 13
rs1799889
SERPINE1
0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs3736234
OLR1
0.851 0.040 12 10160535 non coding transcript exon variant G/A snv 0.40 4
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs974819 0.807 0.080 11 103789839 intron variant T/A;C snv 6
rs539179964
RIMS2
0.882 0.080 8 104248720 missense variant C/T snv 1.6E-05 4.2E-05 3
rs4925
GSTO1
0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
rs28937313
ABCA1
0.882 0.160 9 104822520 missense variant T/C snv 8.0E-06 3
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13
rs4149313
ABCA1
0.763 0.240 9 104824472 missense variant T/C snv 9
rs2066715
ABCA1
0.807 0.160 9 104825752 missense variant C/T snv 8.2E-02 5.5E-02 7
rs2230806
ABCA1
0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs17398575 0.882 0.040 7 106769006 intron variant G/A snv 0.20 3
rs6601530
PINX1
1.000 0.040 8 10813762 intron variant G/A snv 0.61 1
rs3900940
MYH15
0.827 0.040 3 108428881 missense variant T/A;C snv 4.3E-06; 0.24 6
rs2228315
SELPLG
0.807 0.120 12 108624122 missense variant C/T snv 0.11 0.14 7
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs4773144
COL4A1 ; COL4A2
0.827 0.080 13 110308365 intron variant A/G snv 0.42 7
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs879254582
LDLR
0.851 0.160 19 11105488 frameshift variant AGCCCCT/- delins 4
rs879254693
LDLR
0.807 0.160 19 11107424 missense variant T/A;C;G snv 7
rs879254840
LDLR ; MIR6886
0.827 0.120 19 11113322 missense variant A/G snv 5
rs879254850
MIR6886 ; LDLR
0.776 0.160 19 11113365 missense variant A/G;T snv 4.0E-06 9