Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
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
rs11053646
OLR1
0.724 0.280 12 10160849 missense variant C/G snv 0.11 0.13 18
rs11057830
SCARB1
0.851 0.040 12 124822507 intron variant G/A snv 0.15 5
rs1129293
PIK3CG
0.882 0.040 7 106872566 synonymous variant C/T snv 0.32 0.26 3
rs11638352
FRMD5
0.925 0.040 15 44000939 intron variant C/A;G snv 2
rs117714106 0.882 0.080 14 84338144 intergenic variant C/T snv 9.1E-03 3
rs11915606
BTD
0.925 0.040 3 15633655 intron variant T/G snv 3.4E-02 2
rs1202989817
SOD1 ; LOC102724449
0.716 0.360 21 31659813 missense variant T/C;G snv 8.0E-06 7.0E-06 18
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs12290663 0.925 0.040 11 26141193 intergenic variant G/A snv 5.7E-02 2
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs12696304 0.776 0.320 3 169763483 downstream gene variant C/G snv 0.38 10
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 16
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
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