Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs138760780
CDK18
0.882 0.040 1 205515245 intron variant C/T snv 1.5E-02 3
rs1408888
DACH1
0.851 0.120 13 71854515 intron variant T/G snv 0.30 5
rs1466535
LRP1
0.790 0.160 12 57140687 intron variant G/A;C snv 9
rs1467568
SIRT1
0.776 0.320 10 67915401 intron variant A/G snv 0.46 8
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs16941382
GOSR2 ; LRRC37A2
0.882 0.040 17 46966142 intron variant T/C snv 0.15 3
rs17251221
CASR
0.724 0.360 3 122274400 intron variant A/G snv 0.11 18
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 12
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
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs1761667
CD36
0.752 0.320 7 80615623 intron variant G/A snv 0.49 12
rs17757541
BCL2
0.827 0.240 18 63212453 intron variant C/G;T snv 7
rs1790349
DHCR7
0.882 0.040 11 71431304 intron variant T/C snv 0.19 4
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs182052
ADIPOQ
0.701 0.440 3 186842993 intron variant G/A snv 0.38 19
rs1830321
TEX41 ; LOC100505498
0.827 0.080 2 145067988 intron variant C/T snv 0.40 5
rs184003
AGER
0.724 0.400 6 32182519 intron variant C/A snv 0.12 0.12 15
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs2106261
ZFHX3
0.763 0.160 16 73017721 intron variant C/G;T snv 11
rs2144300
GALNT2
0.882 0.040 1 230159169 intron variant C/T snv 0.44 7