Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12663103
GPSM3
0.851 0.240 6 32193547 intron variant T/C snv 6.1E-02 7
rs12785878
NADSYN1
0.677 0.520 11 71456403 intron variant G/A;T snv 25
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2523535 0.851 0.200 6 31368473 intron variant A/G snv 0.32 7
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 10
rs3130933
POU5F1 ; TCF19
0.882 0.200 6 31164308 intron variant T/C snv 0.92 3
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs492899
CYP21A2 ; SKIV2L
0.882 0.240 6 31965741 intron variant T/C snv 0.12 0.15 4
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs909253
LTA ; LOC100287329
0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs10811661 0.724 0.400 9 22134095 intergenic variant T/C snv 0.14 22
rs204999 0.763 0.480 6 32142202 intergenic variant A/G snv 0.28 13
rs3130361 0.925 0.160 6 30371787 intergenic variant A/G snv 0.81 3
rs423639 0.882 0.240 6 33019997 intergenic variant C/T snv 0.11 3
rs2508015 0.925 0.160 6 31042423 regulatory region variant G/A;C snv 2
rs5219
KCNJ11
0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs1041981
LOC100287329 ; LTA
0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 25
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 14
rs1131498
C1orf112 ; SELL
0.732 0.360 1 169707345 missense variant A/G snv 0.21 0.22 13
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100