Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1409785 1.000 0.040 1 74782438 intergenic variant G/A snv 0.65 2
rs2239647
AKAP6
0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65 7
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
rs7124728
SHANK2
1.000 0.040 11 71165389 intron variant T/C snv 0.64 1
rs2853677
TERT
0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 19
rs10764901
LOC105378560 ; MGMT
1.000 0.040 10 129716598 intron variant A/G snv 0.62 1
rs10116277
CDKN2B-AS1
0.827 0.160 9 22081398 intron variant G/T snv 0.62 8
rs7216389
GSDMB
0.732 0.440 17 39913696 intron variant C/T snv 0.60 14
rs1005230
VEGFA
0.827 0.040 6 43768759 upstream gene variant T/C snv 0.60 5
rs11506105
EGFR
0.851 0.160 7 55152484 intron variant A/G snv 0.59 4
rs145929329
CDKN2B-AS1
0.882 0.040 9 22066213 intron variant TTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTTTTT delins 0.58 3
rs7049105
CDKN2B-AS1
0.807 0.120 9 22028802 intron variant A/G snv 0.58 7
rs11603023
PHLDB1
0.925 0.120 11 118615352 intron variant T/C snv 0.57 3
rs920778
HOTAIR
0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs494560
PHLDB1
1.000 0.040 11 118650844 non coding transcript exon variant A/G snv 0.57 1
rs7107785
MAML2
1.000 0.040 11 96014174 intron variant T/C snv 0.57 2
rs573905
LOC105369519
1.000 0.040 11 118701558 intron variant A/G snv 0.56 1
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs7904519
TCF7L2
0.763 0.240 10 113014168 intron variant A/G snv 0.55 9
rs699473
SOD3
0.827 0.160 4 24795181 intron variant C/T snv 0.54 5
rs2194492
NMI
1.000 0.040 2 151289680 5 prime UTR variant G/C snv 0.53 1
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs723527
EGFR
0.882 0.040 7 55067179 intron variant A/G snv 0.53 4
rs843720
ACYP2 ; LOC105374610
0.752 0.280 2 54283523 intron variant T/G snv 0.52 10