Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1537378
CDKN2B-AS1
0.882 0.160 9 22061615 intron variant A/G snv 0.73 4
rs6475604
CDKN2B-AS1
0.925 0.040 9 22052735 intron variant T/C snv 0.72 3
rs7030641
CDKN2B-AS1
1.000 0.040 9 22054041 intron variant C/T snv 0.72 2
rs1360589
CDKN2B-AS1
1.000 0.040 9 22045318 intron variant C/T snv 0.72 2
rs2157719
CDKN2B-AS1
0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 17
rs1333037
CDKN2B-AS1
0.925 0.040 9 22040766 intron variant C/T snv 0.71 3
rs7866783
CDKN2B-AS1
1.000 0.040 9 22056360 non coding transcript exon variant A/G snv 0.71 2
rs1556515
CDKN2B-AS1
1.000 0.040 9 22036368 non coding transcript exon variant C/T snv 0.71 2
rs1008878
CDKN2B-AS1
1.000 0.040 9 22036113 non coding transcript exon variant G/T snv 0.71 2
rs2069418
CDKN2B-AS1 ; CDKN2B
1.000 0.040 9 22009699 intron variant G/C snv 0.70 2
rs4451405
CDKN2B-AS1
9 22071751 intron variant C/T snv 0.69 1
rs7341786
CDKN2B-AS1
9 22112242 intron variant A/C snv 0.65 2
rs7341791
CDKN2B-AS1
9 22112428 intron variant A/G snv 0.65 1
rs1537374
CDKN2B-AS1
1.000 0.040 9 22116047 intron variant A/G snv 0.64 3
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs4977756
CDKN2B-AS1
0.683 0.440 9 22068653 intron variant G/A snv 0.64 24
rs7859362
CDKN2B-AS1
9 22105928 intron variant T/C snv 0.64 2
rs1412834
CDKN2B-AS1
0.790 0.080 9 22110132 intron variant T/C snv 0.64 11
rs1333043
CDKN2B-AS1
9 22106732 intron variant T/A snv 0.64 2
rs10733376
CDKN2B-AS1
1.000 0.080 9 22114470 intron variant G/C snv 0.64 3
rs7857118
CDKN2B-AS1
9 22124141 intron variant A/T snv 0.64 1
rs10965224
CDKN2B-AS1
1.000 0.040 9 22067277 intron variant T/A snv 0.64 2
rs2184061
CDKN2B-AS1
1.000 0.040 9 22061563 intron variant C/A;T snv 0.64 2
rs1333042
CDKN2B-AS1
0.827 0.120 9 22103814 intron variant A/G snv 0.63 7
rs1333047
CDKN2B-AS1
0.790 0.240 9 22124505 intron variant A/T snv 0.63 9