Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10757279
CDKN2B-AS1
0.925 0.040 9 22124631 intron variant A/G snv 0.40 3
rs10811656
CDKN2B-AS1
0.807 0.200 9 22124473 intron variant C/T snv 0.47 7
rs11057830
SCARB1
0.851 0.040 12 124822507 intron variant G/A snv 0.15 5
rs11638352
FRMD5
0.925 0.040 15 44000939 intron variant C/A;G snv 2
rs11915606
BTD
0.925 0.040 3 15633655 intron variant T/G snv 3.4E-02 2
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs138741635
FHIT
0.925 0.040 3 60942161 intron variant T/A;G snv 2
rs144610116
FAM114A1
0.925 0.040 4 38941227 intron variant T/C snv 8.6E-03 2
rs145044782
GLCCI1
0.925 0.040 7 7995866 intron variant G/A snv 2.9E-02 2
rs147204125
ACOT6
0.925 0.040 14 73609035 intron variant A/G snv 9.8E-03 2
rs147233090
CATSPER2P1
0.925 0.040 15 43735849 intron variant C/T snv 1.7E-02 6
rs148121703
GABRB1
0.925 0.040 4 47371654 intron variant TGT/- delins 2.6E-03 2
rs151269874
TMEM231
0.925 0.040 16 75549741 intron variant C/T snv 6.2E-03 2
rs17398575 0.882 0.040 7 106769006 intron variant G/A snv 0.20 3
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs181937009
LOC107986652 ; LOC100507477
0.925 0.040 6 140064258 intron variant A/G snv 0.23 3
rs190543502
TP53BP1
0.925 0.040 15 43464986 intron variant T/A;C snv 2
rs1994016
ADAMTS7
0.851 0.160 15 78787892 intron variant C/T snv 0.30 7
rs201052613 0.882 0.080 1 173026503 intron variant T/-;TT delins 9.4E-03 3
rs2070744
NOS3
0.608 0.680 7 150992991 intron variant C/T snv 0.70 54
rs2733201
FRMD5
0.925 0.040 15 44116203 intron variant T/A;C snv 2
rs3850641
TNFSF4
0.716 0.400 1 173206693 intron variant A/G snv 0.14 17