Disease: Coronary heart disease
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10738609
CDKN2B-AS1
1.000 0.040 9 22114496 intron variant A/C;G;T snv 3
rs10738610
CDKN2B-AS1
0.882 0.120 9 22123767 intron variant A/C;T snv 5
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 13
rs1537372
CDKN2B-AS1
0.752 0.120 9 22103184 intron variant G/A;T snv 14
rs2383205
CDKN2B-AS1
0.925 0.080 9 22060936 intron variant A/C;G snv 3
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs7865618
CDKN2B-AS1
0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 11
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 10
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs564398
CDKN2B-AS1
0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 18
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs3217992
CDKN2B-AS1 ; CDKN2B
0.683 0.480 9 22003224 3 prime UTR variant C/T snv 0.32 22
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 11
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10757277
CDKN2B-AS1
1.000 0.040 9 22124451 intron variant A/G snv 0.40 2
rs10757279
CDKN2B-AS1
0.925 0.040 9 22124631 intron variant A/G snv 0.40 3
rs2891168
CDKN2B-AS1
0.851 0.160 9 22098620 intron variant A/G snv 0.40 5
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs10757272
CDKN2B-AS1
0.851 0.160 9 22088261 intron variant C/T snv 0.41 6
rs10738606
CDKN2B-AS1
1.000 0.040 9 22088091 intron variant A/T snv 0.42 2
rs1333046
CDKN2B-AS1
0.925 0.080 9 22124124 intron variant T/A snv 0.43 4
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs10811656
CDKN2B-AS1
0.807 0.200 9 22124473 intron variant C/T snv 0.47 7