Disease: Coronary Artery Disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1056515
RGS5
0.882 0.040 1 163143470 3 prime UTR variant G/T snv 0.37 3
rs12347433
DELEC1 ; TNC
0.882 0.040 9 115035318 synonymous variant T/C snv 0.23 0.21 3
rs2269422
AGER
0.882 0.040 6 32183517 intron variant T/C snv 1.7E-02 5.8E-03 3
rs7833904 0.882 0.040 8 58505103 upstream gene variant A/T snv 0.55 3
rs79681911
SAA1
0.882 0.040 11 18269755 missense variant G/A snv 2.1E-03 8.0E-04 3
rs8042271 0.882 0.040 15 89030987 intergenic variant G/A;T snv 3
rs121918313
LRP6 ; BCL2L14
0.851 0.080 12 12164494 missense variant G/A snv 1.6E-05 4
rs12762303
ALOX5
0.851 0.080 10 45373723 upstream gene variant T/C snv 0.17 4
rs1867624 0.851 0.080 17 64309731 upstream gene variant C/T snv 0.65 4
rs3736234
OLR1
0.851 0.040 12 10160535 non coding transcript exon variant G/A snv 0.40 4
rs4888378
CFDP1
0.851 0.040 16 75298143 intron variant A/G snv 0.52 4
rs1384889210
APOA1 ; APOA1-AS
0.827 0.040 11 116836193 missense variant C/A snv 5
rs2298566
SNX19
0.827 0.040 11 130880747 missense variant A/C;T snv 0.77; 4.0E-06 5
rs2820315
LMOD1
0.882 0.040 1 201903136 intron variant C/T snv 0.23 5
rs4252120
PLG
0.827 0.080 6 160722576 intron variant T/C;G snv 0.21 5
rs7217186
ALOX15
0.827 0.120 17 4636097 intron variant C/T snv 0.45 5
rs9289231
KALRN
0.827 0.120 3 124055231 intergenic variant T/G snv 0.15 5
rs1264352930
APOA1 ; APOA1-AS
0.807 0.120 11 116836082 missense variant C/A snv 4.2E-06 6
rs2453021
TNFRSF9
0.807 0.080 1 7929506 intron variant C/A;T snv 6
rs2943650 0.827 0.120 2 226241205 intergenic variant C/T snv 0.58 6
rs3900940
MYH15
0.827 0.040 3 108428881 missense variant T/A;C snv 4.3E-06; 0.24 6
rs7439293
PALLD
0.807 0.080 4 168756335 non coding transcript exon variant G/A snv 0.44 6
rs974819 0.807 0.080 11 103789839 intron variant T/A;C snv 6
rs1010
VAMP8
0.807 0.120 2 85581859 3 prime UTR variant T/C;G snv 7
rs16933090
SOX6
0.790 0.160 11 16434247 5 prime UTR variant C/T snv 0.12 7