Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs11669133
SMARCA4
1.000 0.040 19 10981463 intron variant G/A snv 4.2E-02 2
rs11671653
DNM2
1.000 0.040 19 10727810 intron variant G/A;T snv 2
rs12654264
HMGCR
0.925 0.120 5 75352778 intron variant A/T snv 0.38 7
rs12670798
DNAH11 ; LOC105375183
1.000 0.040 7 21567734 intron variant T/C snv 0.26 5
rs13161895
RNF130
1.000 0.040 5 180044201 intron variant C/T snv 0.12 2
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 14
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs174570
FADS2
0.882 0.200 11 61829740 intron variant C/T snv 0.15 11
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 13
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs2254287
COL11A2
1.000 0.040 6 33176171 intron variant C/A;G;T snv 3
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 10
rs2954029 0.807 0.160 8 125478730 intron variant A/T snv 0.42 14
rs3846663
HMGCR ; CERT1
0.882 0.120 5 75359901 intron variant C/T snv 0.35 7
rs4844614
CR1L
1.000 0.040 1 207701830 intron variant G/C;T snv 3
rs5031002
AR
1.000 0.040 X 67722783 intron variant G/A snv 1.5E-02 1.5E-02 3
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 10
rs6601299
LOC157273
0.925 0.040 8 9327181 intron variant T/C snv 0.88 5
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18