Disease: Atherosclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs915014
C1orf167 ; MTHFR
0.925 0.040 1 11789412 missense variant T/C snv 2
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
rs1298417395
COP1
0.882 0.080 1 176206716 missense variant C/T snv 1.4E-05 4
rs1440763451
PPARG
0.882 0.080 3 12416849 missense variant A/G snv 4.0E-06 4
rs1490867890
MCL1 ; LOC107985203
0.882 0.080 1 150579475 missense variant G/A;C snv 3
rs1866389
THBS4
0.790 0.080 5 80065442 missense variant G/C snv 0.17 0.17 9
rs1867624 0.851 0.080 17 64309731 upstream gene variant C/T snv 0.65 4
rs201989364
ADIPOQ-AS1 ; ADIPOQ
0.882 0.080 3 186854295 missense variant A/G snv 6.4E-05 2.1E-05 3
rs2229116
RYR3
0.827 0.080 15 33613209 missense variant A/G snv 0.23 0.21 9
rs2229238
IL6R
0.851 0.080 1 154465420 3 prime UTR variant T/A;C snv 0.80 5
rs2453021
TNFRSF9
0.807 0.080 1 7929506 intron variant C/A;T snv 6
rs28362286
PCSK9
0.851 0.080 1 55063542 stop gained C/A;T snv 5.6E-04 6
rs4076317
ANGPTL4
0.882 0.080 19 8364115 intron variant C/G snv 0.25 5
rs4252120
PLG
0.827 0.080 6 160722576 intron variant T/C;G snv 0.21 5
rs4773144
COL4A1 ; COL4A2
0.827 0.080 13 110308365 intron variant A/G snv 0.42 7
rs4845617
IL6R-AS1 ; IL6R
0.882 0.080 1 154405422 5 prime UTR variant G/A;C snv 4
rs4862423
ACSL1
0.882 0.080 4 184805394 intron variant C/T snv 0.37 4
rs537765533
IL1RN
0.882 0.080 2 113132839 missense variant G/C snv 2.0E-05 3
rs539179964
RIMS2
0.882 0.080 8 104248720 missense variant C/T snv 1.6E-05 4.2E-05 3
rs6666258
KCNN3
0.882 0.080 1 154841792 intron variant G/C snv 0.30 3
rs67608943
PCSK9
0.851 0.080 1 55046549 stop gained C/G;T snv 1.9E-04 8