Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 25
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs3747093
YDJC
0.732 0.200 22 21630090 upstream gene variant G/A snv 0.32 16
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs7705526
TERT
0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs13331259
FAM234A
16 249924 intron variant A/G snv 3.0E-02 14
rs7385804
TFR2
0.851 0.120 7 100638347 intron variant C/A snv 0.65 14
rs7775698
HBS1L
1.000 0.080 6 135097497 intron variant C/T snv 6.9E-02 14
rs28601761 1.000 0.040 8 125487789 intron variant C/G snv 0.37 13
rs58658771 0.776 0.080 15 32709533 intergenic variant T/A snv 0.20 13
rs7776054
HBS1L
6 135097778 intron variant A/G snv 0.24 13
rs9399137
HBS1L
0.851 0.320 6 135097880 intron variant T/C snv 0.20 13
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs140522
ODF3B
0.851 0.160 22 50532837 upstream gene variant T/A;C snv 11
rs2179593
TOX2
0.790 0.080 20 44031646 intron variant C/A snv 0.71 11
rs9494145 0.925 0.080 6 135111414 intergenic variant T/A;C snv 11
rs12638862 0.827 0.160 3 169759718 downstream gene variant A/G snv 0.24 10
rs17758695
BCL2
18 63253621 intron variant C/T snv 2.1E-02 10
rs218265 4 54542832 intergenic variant T/C snv 0.21 10
rs4895441
LOC105378010
0.925 0.080 6 135105435 upstream gene variant A/G snv 0.21 10
rs9376092
LOC105378010
0.851 0.120 6 135106006 upstream gene variant C/A snv 0.24 10
rs9977672 0.827 0.120 21 39091357 intergenic variant G/A snv 0.22 10