Disease: Arteriosclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1282382243
DLEU7-AS1 ; DLEU1 ; DLEU7
0.807 0.120 13 50843630 missense variant G/A snv 8
rs1403934301
SHBG
0.882 0.120 17 7631317 missense variant G/A snv 3
rs2144908
LOC105372629 ; HNF4A
0.851 0.120 20 44357077 intron variant G/A snv 0.18 5
rs2518136
AHSG
0.851 0.120 3 186620038 intron variant T/C snv 0.46 4
rs46522
UBE2Z
0.807 0.120 17 48911235 non coding transcript exon variant C/T snv 0.40 8
rs116843064
ANGPTL4
0.776 0.160 19 8364439 missense variant G/A snv 1.3E-02 1.5E-02 16
rs16933090
SOX6
0.790 0.160 11 16434247 5 prime UTR variant C/T snv 0.12 7
rs185847354
ADIPOQ ; ADIPOQ-AS1
0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05 11
rs20455
KIF6 ; LOC107986594
0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 18
rs7895340
TCF7L2
0.851 0.160 10 113041766 intron variant G/A snv 0.53 4
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs6495446
MTHFS ; ST20-MTHFS
0.851 0.200 15 79862640 intron variant C/T snv 0.31 6
rs198389
NPPB
0.776 0.240 1 11859214 upstream gene variant A/G snv 0.39 10
rs2066714
ABCA1
0.742 0.240 9 104824472 missense variant T/C snv 0.21 0.25 13
rs773641005
GOT2
0.742 0.240 16 58723829 missense variant T/C snv 14
rs1022113606
SOD3
0.732 0.280 4 24800161 missense variant G/C snv 1.6E-04 2.1E-05 17
rs2230806
ABCA1
0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs2536512
SOD3
0.752 0.280 4 24799693 missense variant G/A;T snv 0.55 14
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs20551
EP300
0.752 0.320 22 41152004 missense variant A/G snv 0.31 0.23 10
rs2295490
TRIB3
0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16
rs660339
UCP2
0.695 0.320 11 73978059 missense variant G/A snv 0.41 0.43 24
rs80356814
LMNA
0.732 0.320 1 156138697 synonymous variant C/T snv 8.0E-06 15