Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9931702
AKTIP
0.851 0.160 16 53492639 non coding transcript exon variant C/T snv 0.55 4
rs9917028
TNFAIP8L1
0.882 0.080 19 4640971 non coding transcript exon variant G/A snv 0.45 3
rs963918
RAD51B
0.827 0.120 14 68595397 3 prime UTR variant C/T snv 0.64 5
rs963917
RAD51B
0.827 0.120 14 68595606 3 prime UTR variant G/A snv 0.26 5
rs953038635
SOD2
0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs9513111
FLT1
0.882 0.080 13 28423426 intron variant C/T snv 0.75 3
rs944309752
TP53BP1
0.882 0.080 15 43421159 synonymous variant G/C snv 7.0E-06 3
rs9344
CCND1
0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 34
rs9302648
AKTIP
0.882 0.080 16 53493869 non coding transcript exon variant G/T snv 0.54 3
rs9298814
IFNA17
0.790 0.160 9 21227623 missense variant A/C;G snv 0.12; 8.8E-06 7
rs9277952 0.851 0.080 6 33236497 upstream gene variant G/A snv 0.10 4
rs9277535
HLA-DPB1
0.724 0.440 6 33087084 3 prime UTR variant A/G snv 0.25 13
rs9272143
HLA-DQA1
0.882 0.080 6 32633026 intron variant T/C snv 0.49 3
rs920778
HOTAIR
0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs895819
MIR23A ; LOC284454 ; MIR27A ; MIR24-2
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs833070
VEGFA
0.776 0.440 6 43774889 non coding transcript exon variant T/C snv 0.58 11
rs833068
VEGFA
0.851 0.120 6 43774790 non coding transcript exon variant G/A snv 0.36 4
rs833061
VEGFA
0.605 0.600 6 43769749 upstream gene variant C/G;T snv 42
rs8179
CDK6
0.882 0.080 7 92606850 3 prime UTR variant T/A;C;G snv 8
rs8076131
ORMDL3
0.790 0.200 17 39924659 intron variant G/A;C snv 11
rs807183
ATG4A
0.851 0.120 X 108094263 intron variant G/A snv 0.51 4
rs807181
PSMD10 ; ATG4A
0.851 0.120 X 108090354 intron variant G/C;T snv 4
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 12