Disease: Cardiovascular Diseases
Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 25
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 22
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 20
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs516246
FUT2 ; LOC105447645
0.925 0.160 19 48702915 intron variant C/T snv 0.38 0.45 10
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 10
rs17482753 1.000 0.080 8 19975135 regulatory region variant G/T snv 8.8E-02 8
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 8
rs1154988 3 136206349 upstream gene variant T/A snv 0.76 7
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs127430
APCDD1L-DT
20 58589799 intron variant A/G;T snv 6
rs1367117
APOB
1.000 0.080 2 21041028 missense variant G/A snv 0.26 0.24 6
rs17411031 0.925 0.120 8 19994799 regulatory region variant C/G snv 0.25 6
rs7890572
IL1RAPL1
X 29622701 intron variant A/G snv 9.3E-02 6
rs12042319
DOCK7
1.000 0.040 1 62584148 3 prime UTR variant G/A snv 0.36 5
rs10769254
MYBPC3
11 47340914 intron variant G/C snv 0.27 4
rs6589567 1.000 0.040 11 116799960 intergenic variant A/C;G;T snv 4
rs78058190 2 218835276 upstream gene variant G/A snv 3.9E-02 4