Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1440763451
PPARG
0.882 0.080 3 12416849 missense variant A/G snv 4.0E-06 4
rs4987262
PTGIR
0.882 0.040 19 46623592 missense variant G/A;C snv 7.1E-03 4
rs877087
RYR3
0.882 0.080 15 33582074 intron variant T/C;G snv 4
rs774887459
SGSM3
0.882 0.080 22 40405776 missense variant G/A snv 4.0E-06 4
rs243330
SOCS1 ; RMI2 ; LOC105371082
0.851 0.240 16 11257134 intron variant C/T snv 0.49 4
rs7895340
TCF7L2
0.851 0.160 10 113041766 intron variant G/A snv 0.53 4
rs16899974
AGXT2
0.827 0.120 5 34998772 missense variant C/A snv 0.24 0.19 5
rs7217186
ALOX15
0.827 0.120 17 4636097 intron variant C/T snv 0.45 5
rs4076317
ANGPTL4
0.882 0.080 19 8364115 intron variant C/G snv 0.25 5
rs1384889210
APOA1 ; APOA1-AS
0.827 0.040 11 116836193 missense variant C/A snv 5
rs140808909
APOE
0.851 0.120 19 44909080 missense variant G/A snv 2.0E-04 5.6E-05 5
rs213045
ECE1
0.851 0.120 1 21290752 intron variant G/T snv 0.44 5
rs2229238
IL6R
0.851 0.080 1 154465420 3 prime UTR variant T/A;C snv 0.80 5
rs879254840
LDLR ; MIR6886
0.827 0.120 19 11113322 missense variant A/G snv 5
rs2820315
LMOD1
0.882 0.040 1 201903136 intron variant C/T snv 0.23 5
rs2144908
LOC105372629 ; HNF4A
0.851 0.120 20 44357077 intron variant G/A snv 0.18 5
rs1249040838
MIR6886 ; LDLR
0.827 0.120 19 11113699 missense variant G/A snv 4.0E-06 5
rs4252120
PLG
0.827 0.080 6 160722576 intron variant T/C;G snv 0.21 5
rs2298566
SNX19
0.827 0.040 11 130880747 missense variant A/C;T snv 0.77; 4.0E-06 5
rs12564445
TNNT2
0.851 0.040 1 201376359 intron variant G/A snv 0.27 5
rs2943650 0.827 0.120 2 226241205 intergenic variant C/T snv 0.58 6
rs974819 0.807 0.080 11 103789839 intron variant T/A;C snv 6
rs1264352930
APOA1 ; APOA1-AS
0.807 0.120 11 116836082 missense variant C/A snv 4.2E-06 6
rs121918393
APOE
0.851 0.120 19 44908756 missense variant C/A;T snv 1.3E-05; 9.0E-05 6
rs353291
CARMN ; MIR145
0.807 0.200 5 149431183 non coding transcript exon variant T/C snv 0.35 6