Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs12290663 0.925 0.040 11 26141193 intergenic variant G/A snv 5.7E-02 2
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
rs144972973 0.925 0.040 15 44272494 intergenic variant A/G snv 1.8E-02 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
rs148121703
GABRB1
0.925 0.040 4 47371654 intron variant TGT/- delins 2.6E-03 2
rs149232047 0.925 0.040 6 126276990 intergenic variant A/G snv 1.5E-04 2
rs151269874
TMEM231
0.925 0.040 16 75549741 intron variant C/T snv 6.2E-03 2
rs16999497 0.925 0.040 X 129601222 regulatory region variant T/C snv 7.8E-02 2
rs189889864 0.925 0.040 9 104634643 downstream gene variant G/A snv 2.8E-03 2
rs190543502
TP53BP1
0.925 0.040 15 43464986 intron variant T/A;C snv 2
rs192427471 0.925 0.040 4 124644124 intergenic variant C/T snv 2.4E-03 2
rs201394051 0.925 0.040 5 117697919 intergenic variant TA/-;TATA;TATATA delins 2
rs2733201
FRMD5
0.925 0.040 15 44116203 intron variant T/A;C snv 2
rs4357117
LOC107986540
0.925 0.040 6 66873865 intergenic variant G/T snv 1.7E-02 2
rs57578064
TOMM5
0.925 0.040 9 37590253 intron variant G/A snv 1.9E-02 2
rs62568141 0.925 0.040 9 77012344 regulatory region variant C/T snv 2.4E-02 2
rs9295128 0.925 0.040 6 160330499 intergenic variant G/T snv 1.1E-02 2
rs10757279
CDKN2B-AS1
0.925 0.040 9 22124631 intron variant A/G snv 0.40 3
rs1129293
PIK3CG
0.882 0.040 7 106872566 synonymous variant C/T snv 0.32 0.26 3
rs117714106 0.882 0.080 14 84338144 intergenic variant C/T snv 9.1E-03 3
rs17398575 0.882 0.040 7 106769006 intron variant G/A snv 0.20 3