Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 4
rs10811650
CDKN2B-AS1
0.882 0.200 9 22067594 intron variant A/G snv 0.37 4
rs10965219
CDKN2B-AS1
0.882 0.080 9 22053688 intron variant A/G snv 0.58 4
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 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
rs1537375
CDKN2B-AS1
0.882 0.120 9 22116072 intron variant T/C;G snv 4
rs9632884
CDKN2B-AS1
0.851 0.160 9 22072302 intron variant G/A;C snv 4
rs1063192
CDKN2B ; CDKN2B-AS1
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 4
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 4
rs10738604
CDKN2B-AS1
1.000 0.040 9 22025494 intron variant G/A snv 0.29 3
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
rs10757269
CDKN2B-AS1
1.000 0.040 9 22072265 intron variant A/C;G snv 3
rs10757272
CDKN2B-AS1
0.851 0.160 9 22088261 intron variant C/T snv 0.41 3
rs10811647
CDKN2B-AS1
1.000 0.040 9 22065003 intron variant C/G;T snv 3
rs10965212
CDKN2B-AS1
0.925 0.080 9 22023796 intron variant T/A;C;G snv 3
rs10965215
CDKN2B-AS1
0.882 0.120 9 22029446 missense variant G/A snv 0.55 0.46 3
rs1333045
CDKN2B-AS1
0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 3
rs2157719
CDKN2B-AS1
0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 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
rs3218020
CDKN2B-AS1
0.882 0.120 9 21997873 intron variant G/A;C snv 3
rs496892
CDKN2B-AS1
0.827 0.160 9 22024352 intron variant C/T snv 0.40 3