Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 23
rs7656411
TLR2
0.790 0.320 4 153706503 downstream gene variant T/G snv 0.35 8
rs8124792
CYP24A1
0.827 0.120 20 54150268 downstream gene variant G/A snv 7.8E-02 6
rs230490
LOC105377621
0.882 0.080 4 102466262 downstream gene variant G/A snv 0.34 3
rs997476 0.882 0.080 4 102620848 downstream gene variant G/T snv 4.3E-02 3
rs10450310
MBL2
0.925 0.080 10 52764898 downstream gene variant G/A snv 0.29 2
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs4950928
CHI3L1
0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs7799039
LOC105375494
0.649 0.560 7 128238730 upstream gene variant G/A;C snv 33
rs10795668
LOC105376400
0.724 0.160 10 8659256 upstream gene variant G/A snv 0.24 17
rs10759932
TLR4
0.732 0.560 9 117702866 upstream gene variant T/C snv 0.18 15
rs12778366
SIRT1
0.724 0.480 10 67883321 upstream gene variant T/C;G snv 13
rs16840252
CTLA4
0.776 0.480 2 203866796 upstream gene variant C/T snv 0.16 8
rs8073069
BIRC5
0.807 0.200 17 78213692 upstream gene variant G/C snv 0.33 7
rs17878467
BIRC5
0.925 0.080 17 78214076 upstream gene variant C/G;T snv 6
rs2853668 0.882 0.080 5 1299910 upstream gene variant G/T snv 0.33 5
rs3093075 0.882 0.120 1 159710123 upstream gene variant G/T snv 0.13 5
rs2770150 0.925 0.080 9 117700861 upstream gene variant A/G snv 0.22 4
rs2243828
MPO
0.925 0.080 17 58281523 upstream gene variant A/G;T snv 2
rs4932178
FURIN
0.925 0.080 15 90868426 upstream gene variant C/T snv 0.32 2
rs9344
CCND1
0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 34
rs603965
CCND1
0.732 0.440 11 69648142 splice region variant G/A snv 14
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36