Disease: Coronary Artery Disease
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 73
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 38
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 36
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 25
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 21
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 8
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 8
rs17630235
TRAFD1
0.925 0.120 12 112153882 downstream gene variant G/A;C snv 7
rs2281727
SMG6
0.882 0.080 17 2214651 intron variant A/G snv 0.38 4
rs2257129
LOC105378522
1.000 0.040 10 121139183 regulatory region variant T/C snv 0.82 3
rs2820315
LMOD1
0.882 0.040 1 201903136 intron variant C/T snv 0.23 3
rs2891403
RPH3A
1.000 0.040 12 112699767 intron variant A/G;T snv 2