Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9933544 0.882 0.040 16 24576962 downstream gene variant A/C snv 0.29 3
rs9841110 1.000 0.040 3 49455048 regulatory region variant C/G snv 0.28 1
rs9656979
CCDC26
1.000 0.040 8 129652161 intron variant T/C snv 0.37 1
rs944797
CDKN2B-AS1
0.882 0.120 9 22115287 intron variant T/C;G snv 0.49 5
rs9288516
XRCC5
0.827 0.120 2 216188541 intron variant T/A snv 5.0E-02 6
rs920778
HOTAIR
0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs891835
CCDC26
0.851 0.120 8 129479506 intron variant T/G snv 0.17 5
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs8753
POLR2A
1.000 0.040 17 7514323 non coding transcript exon variant C/T snv 1.4E-02 2
rs865880036
MEIS2
0.827 0.040 15 37098156 missense variant A/C snv 1.3E-04 5
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs845552
EGFR
1.000 0.040 7 55177814 intron variant A/G snv 0.43 1
rs843720
ACYP2 ; LOC105374610
0.752 0.280 2 54283523 intron variant T/G snv 0.52 10
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs828704
XRCC5
1.000 0.040 2 216128888 intron variant C/A snv 0.81 1
rs8105767
LOC112268248
0.882 0.120 19 22032639 non coding transcript exon variant A/G snv 0.35 3
rs7963551
RAD52
0.807 0.160 12 912349 3 prime UTR variant T/G snv 0.13 7
rs7938889
MAML2
1.000 0.040 11 96231355 intron variant C/T snv 0.48 1
rs7904519
TCF7L2
0.763 0.240 10 113014168 intron variant A/G snv 0.55 9
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs786204929
PTEN
0.752 0.200 10 87933144 stop gained G/A;T snv 12
rs786202398
PTEN
0.925 0.080 10 87925518 stop gained T/A;G snv 2
rs78378222
TP53
0.662 0.360 17 7668434 3 prime UTR variant T/G snv 8.3E-03 37