Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10757272
CDKN2B-AS1
0.851 0.160 9 22088261 intron variant C/T snv 0.41 3
rs2891168
CDKN2B-AS1
0.851 0.160 9 22098620 intron variant A/G snv 0.40 3
rs496892
CDKN2B-AS1
0.827 0.160 9 22024352 intron variant C/T snv 0.40 3
rs1537378
CDKN2B-AS1
0.882 0.160 9 22061615 intron variant A/G snv 0.73 2
rs2383204
CDKN2B-AS1
0.827 0.160 9 22055049 intron variant A/G;T snv 2
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 10
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs7049105
CDKN2B-AS1
0.807 0.120 9 22028802 intron variant A/G snv 0.58 5
rs944797
CDKN2B-AS1
0.882 0.120 9 22115287 intron variant T/C;G snv 0.49 5
rs1333042
CDKN2B-AS1
0.827 0.120 9 22103814 intron variant A/G snv 0.63 4
rs1537375
CDKN2B-AS1
0.882 0.120 9 22116072 intron variant T/C;G snv 4
rs10738610
CDKN2B-AS1
0.882 0.120 9 22123767 intron variant A/C;T snv 3
rs10965215
CDKN2B-AS1
0.882 0.120 9 22029446 missense variant G/A snv 0.55 0.46 3
rs3218020
CDKN2B-AS1
0.882 0.120 9 21997873 intron variant G/A;C snv 3
rs615552
CDKN2B-AS1
0.925 0.120 9 22026078 intron variant T/C snv 0.29 3
rs944801
CDKN2B-AS1
0.882 0.120 9 22051671 intron variant G/A;C snv 3
rs10738605
CDKN2B-AS1
0.925 0.120 9 22049131 non coding transcript exon variant C/A;G snv 2
rs1537372
CDKN2B-AS1
0.752 0.120 9 22103184 intron variant G/A;T snv 2
rs10889332
DOCK7
1.000 0.120 1 62485187 3 prime UTR variant C/T snv 0.39 1
rs1537373
CDKN2B-AS1
0.925 0.120 9 22103342 intron variant T/G snv 0.63 1
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 9
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 7
rs173539 0.882 0.080 16 56954132 intergenic variant C/T snv 0.33 7
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 7