Disease: Coronary heart disease
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 8
rs564398
CDKN2B-AS1
0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 7
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 6
rs6475606
CDKN2B-AS1
0.882 0.080 9 22081851 intron variant C/T snv 0.62 5
rs7865618
CDKN2B-AS1
0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 5
rs944797
CDKN2B-AS1
0.882 0.120 9 22115287 intron variant T/C;G snv 0.49 5
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs1333042
CDKN2B-AS1
0.827 0.120 9 22103814 intron variant A/G snv 0.63 4
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 4
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 4
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 3
rs10757272
CDKN2B-AS1
0.851 0.160 9 22088261 intron variant C/T snv 0.41 3
rs1333045
CDKN2B-AS1
0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 3
rs2383206
CDKN2B-AS1
0.742 0.320 9 22115027 intron variant A/G snv 0.49 3
rs2891168
CDKN2B-AS1
0.851 0.160 9 22098620 intron variant A/G snv 0.40 3
rs10217586
CDKN2B-AS1
1.000 0.040 9 22121350 intron variant A/T snv 0.52 2
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 2
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 2
rs1537372
CDKN2B-AS1
0.752 0.120 9 22103184 intron variant G/A;T snv 2
rs1537376
CDKN2B-AS1
1.000 0.040 9 22116221 intron variant T/C snv 0.49 2