Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1265538677
CPB2-AS1 ; CPB2
0.790 0.200 13 46055808 synonymous variant A/G snv 4.0E-06 10
rs137852912
PCSK9
0.776 0.120 1 55057454 missense variant G/A;C;T snv 7.2E-05 10
rs711752
CETP
1.000 0.040 16 56962299 splice region variant G/A;C snv 10
rs573658040
APOE
0.790 0.200 19 44908705 missense variant C/G;T snv 6.3E-06 9
rs763000109
TNF
0.827 0.240 6 31575788 missense variant C/G;T snv 4.1E-06; 1.6E-05 9
rs2297508
SREBF1
0.790 0.240 17 17812003 synonymous variant C/G;T snv 0.50; 7.5E-05 8
rs5030718
TLR4
0.827 0.200 9 117713548 stop gained G/A;T snv 3.1E-03; 8.0E-06 8
rs28942111
PCSK9
0.807 0.120 1 55044016 missense variant T/A snv 7
rs2072183
NPC1L1
0.925 0.040 7 44539581 synonymous variant G/A;C snv 4.0E-06; 0.25 6
rs544453230
LDLR
0.882 0.080 19 11110714 missense variant G/A;C snv 2.8E-05; 4.0E-06 6
rs2229238
IL6R
0.851 0.080 1 154465420 3 prime UTR variant T/A;C snv 0.80 5
rs2281997
ENHO
0.882 0.240 9 34521869 intron variant T/A;C snv 5
rs2292318
SLC12A4
0.925 0.120 16 67951803 intron variant C/A;T snv 0.15 5
rs730882082
LDLR
0.882 0.080 19 11105315 missense variant G/A;T snv 1.6E-05 5
rs739837
VDR
0.882 0.200 12 47844438 3 prime UTR variant G/C;T snv 5
rs879254535
LDLR
0.925 0.080 19 11105369 missense variant T/A;C;G snv 5
rs2297322
SLC15A1
1.000 0.040 13 98723927 missense variant C/G;T snv 0.22 4
rs258
LPL
8 19954741 intron variant G/A;C;T snv 4
rs3755166
LRP2
1.000 0.080 2 169363371 upstream gene variant A/C;G snv 4
rs387906567
APOE
0.882 0.200 19 44908774 missense variant C/G;T snv 6.3E-06 4
rs4240157
ACE2
0.925 0.080 X 15568841 intron variant C/T snv 4
rs4845617
IL6R-AS1 ; IL6R
0.882 0.080 1 154405422 5 prime UTR variant G/A;C snv 4
rs879922
ACE2
0.882 0.160 X 15572684 intron variant C/G snv 4
rs1211098985
MTRR
1.000 0.040 5 7878128 missense variant T/C;G snv 4.0E-06 3
rs1746661
FNDC5
0.925 0.080 1 32869438 intron variant G/A;T snv 3