Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2479409
PCSK9
1.000 0.040 1 55038977 upstream gene variant G/A snv 0.66 4
rs7025486
DAB2IP
0.851 0.040 9 121660124 intron variant G/A snv 0.28 4
rs8087799 0.882 0.080 18 22605468 regulatory region variant G/A snv 0.43 3
rs919433
ANKRD44 ; ANKRD44-IT1
0.882 0.080 2 197301841 intron variant G/A snv 0.38 3
rs137854485
FBN1
0.925 0.160 15 48515402 missense variant G/A snv 2
rs10758278
PHF24
1.000 0.040 9 34825306 intron variant G/A snv 0.53 1
rs3781590
LRP5
1.000 0.040 11 68391684 intron variant G/A snv 0.35 1
rs767169659
MYLK
1.000 0.040 3 123733800 missense variant G/A snv 1.2E-05 1
rs8125581
MMP9
1.000 0.040 20 46010604 missense variant G/A snv 3.0E-04 3.4E-04 1
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs1466535
LRP1
0.790 0.160 12 57140687 intron variant G/A;C snv 9
rs764522
TGFBR2 ; LOC105377015
0.882 0.080 3 30605058 upstream gene variant G/A;C snv 3
rs201191171
SLC12A5-AS1 ; MMP9
0.925 0.080 20 46013279 missense variant G/A;C;T snv 4.0E-06; 4.0E-06 2
rs3091244
CRP
0.724 0.280 1 159714875 upstream gene variant G/A;T snv 17
rs58749629
PCIF1
1.000 0.040 20 45942678 intron variant G/A;T snv 0.13 1
rs77294580
ACE
1.000 0.040 17 63480396 missense variant G/A;T snv 4.0E-06; 4.0E-06 1
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1385526
LRP1
1.000 0.040 12 57138966 intron variant G/C snv 0.26 1
rs782591769
ELN
1.000 0.040 7 74045237 missense variant G/C snv 8.0E-06 1
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs7866503
CDKN2B-AS1
0.882 0.080 9 22091925 intron variant G/T snv 0.50 3
rs4988300
LRP5
0.925 0.120 11 68321363 intron variant G/T snv 0.50 2
rs2652106
VCAN
1.000 0.040 5 83498217 intron variant G/T snv 0.39 1
rs4916251
DNM3 ; PIGC
0.882 0.040 1 172377256 intron variant T/A snv 0.70 3
rs1417938
CRP
0.776 0.320 1 159714396 intron variant T/A;C snv 0.28 10