Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs115689251
LOC107985068
1.000 0.080 17 36032377 intergenic variant A/C snv 1.0E-02 2
rs7341786
CDKN2B-AS1
9 22112242 intron variant A/C snv 0.65 2
rs10757269
CDKN2B-AS1
1.000 0.040 9 22072265 intron variant A/C;G snv 4
rs2383205
CDKN2B-AS1
0.925 0.080 9 22060936 intron variant A/C;G snv 3
rs10757270
CDKN2B-AS1
1.000 0.040 9 22072720 intron variant A/C;G snv 0.40 2
rs6506900
LOC105372049
1.000 0.080 18 31226433 intergenic variant A/C;G snv 2
rs7442201
NSG1
1.000 0.080 4 4360022 intron variant A/C;G snv 2
rs10738609
CDKN2B-AS1
1.000 0.040 9 22114496 intron variant A/C;G;T snv 3
rs6754498
LOC107985783
1.000 0.080 2 185953121 non coding transcript exon variant A/C;G;T snv 2
rs10738610
CDKN2B-AS1
0.882 0.120 9 22123767 intron variant A/C;T snv 5
rs1004638
CDKN2B-AS1
1.000 0.040 9 22115590 intron variant A/C;T snv 3
rs543830
CDKN2B-AS1
1.000 0.040 9 22026640 intron variant A/C;T snv 2
rs7092929
LOC105376360 ; LINC02669
10 3496602 splice region variant A/C;T snv 1
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10757274
CDKN2B-AS1
0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs9349379
PHACTR1
0.732 0.200 6 12903725 intron variant A/G snv 0.32 19
rs2383206
CDKN2B-AS1
0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28 14
rs4841132
LOC157273
8 9326086 non coding transcript exon variant A/G snv 0.89 14
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 10
rs1333042
CDKN2B-AS1
0.827 0.120 9 22103814 intron variant A/G snv 0.63 7
rs523096
CDKN2B-AS1
0.827 0.080 9 22019130 intron variant A/G snv 0.30 7
rs7049105
CDKN2B-AS1
0.807 0.120 9 22028802 intron variant A/G snv 0.58 7