Disease: Arteriosclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1008438
HSPA1L ; HSPA1A
0.807 0.120 6 31815431 upstream gene variant A/C;T snv 6
rs1010
VAMP8
0.807 0.120 2 85581859 3 prime UTR variant T/C;G snv 7
rs1020608562
CCR5AS ; CCR5
0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 9
rs1043618
HSPA1L ; HSPA1A
0.752 0.280 6 31815730 5 prime UTR variant G/A;C;T snv 0.39; 2.0E-05; 4.0E-06 10
rs112735431
RNF213 ; RNF213-AS1
0.683 0.320 17 80385145 missense variant G/A;C snv 2.6E-04; 8.0E-06 24
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs118204057
LPL
0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 16
rs12190287
TCF21
0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 19
rs121918313
LRP6 ; BCL2L14
0.851 0.080 12 12164494 missense variant G/A snv 1.6E-05 4
rs121918393
APOE
0.851 0.120 19 44908756 missense variant C/A;T snv 1.3E-05; 9.0E-05 6
rs1232898090
PPARA
0.637 0.600 22 46198429 missense variant G/C;T snv 4.0E-06; 4.0E-06 40
rs1249040838
MIR6886 ; LDLR
0.827 0.120 19 11113699 missense variant G/A snv 4.0E-06 5
rs1264352930
APOA1 ; APOA1-AS
0.807 0.120 11 116836082 missense variant C/A snv 4.2E-06 6
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1282382243
DLEU7-AS1 ; DLEU1 ; DLEU7
0.807 0.120 13 50843630 missense variant G/A snv 8
rs137852912
PCSK9
0.776 0.120 1 55057454 missense variant G/A;C;T snv 7.2E-05 10
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs1384889210
APOA1 ; APOA1-AS
0.827 0.040 11 116836193 missense variant C/A snv 5
rs1403934301
SHBG
0.882 0.120 17 7631317 missense variant G/A snv 3
rs1440763451
PPARG
0.882 0.080 3 12416849 missense variant A/G snv 4.0E-06 4
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs1458766475
C1orf112 ; SELE
0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs1490867890
MCL1 ; LOC107985203
0.882 0.080 1 150579475 missense variant G/A;C snv 3
rs1535045
CD40
0.742 0.360 20 46119460 intron variant C/A;G;T snv 12