Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 18
rs1537372
CDKN2B-AS1
0.752 0.120 9 22103184 intron variant G/A;T snv 11
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 7
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 5
rs10738607
CDKN2B-AS1
0.925 0.080 9 22088095 intron variant A/G snv 0.42 3
rs10811652
CDKN2B-AS1
0.882 0.120 9 22077086 intron variant A/C;T snv 3
rs1333045
CDKN2B-AS1
0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 3
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28 3
rs4977574
CDKN2B-AS1
0.695 0.520 9 22098575 intron variant A/G;T snv 3
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 2
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 2
rs1333042
CDKN2B-AS1
0.827 0.120 9 22103814 intron variant A/G snv 0.63 2
rs2891168
CDKN2B-AS1
0.851 0.160 9 22098620 intron variant A/G snv 0.40 2
rs564398
CDKN2B-AS1
0.716 0.360 9 22029548 3 prime UTR variant T/C snv 0.31 0.28 2
rs7865618
CDKN2B-AS1
0.776 0.240 9 22031006 non coding transcript exon variant G/A;T snv 2
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 1
rs1333047
CDKN2B-AS1
0.790 0.240 9 22124505 intron variant A/T snv 0.63 1
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 1
rs4977575
CDKN2B-AS1
1.000 0.040 9 22124745 intron variant C/G;T snv 1
rs523096
CDKN2B-AS1
0.827 0.080 9 22019130 intron variant A/G snv 0.30 1
rs6475606
CDKN2B-AS1
0.882 0.080 9 22081851 intron variant C/T snv 0.62 1
rs9632884
CDKN2B-AS1
0.851 0.160 9 22072302 intron variant G/A;C snv 1
rs3217978
CDKN2B ; CDKN2B-AS1
1.000 0.040 9 22007331 intron variant C/A snv 1.2E-02 1