Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2295080
MTOR
0.695 0.320 1 11262571 upstream gene variant G/C;T snv 20
rs16260
CDH1
0.716 0.440 16 68737131 upstream gene variant C/A snv 0.24 18
rs4796793
STAT3
0.716 0.320 17 42390192 upstream gene variant G/C snv 0.67 16
rs2735940
TERT
0.689 0.400 5 1296371 upstream gene variant A/G snv 0.49 14
rs3747093
YDJC
0.732 0.200 22 21630090 upstream gene variant G/A snv 0.32 14
rs874945 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 14
rs12778366
SIRT1
0.724 0.480 10 67883321 upstream gene variant T/C;G snv 13
rs16949649
NME1 ; NME1-NME2
0.776 0.200 17 51152947 upstream gene variant T/C snv 0.39 12
rs2233406
NFKBIA
0.732 0.440 14 35405593 upstream gene variant G/A snv 0.26 12
rs3102735
COLEC10 ; TNFRSF11B
0.752 0.400 8 118952831 upstream gene variant T/C snv 0.17 12
rs733618
CTLA4
0.763 0.440 2 203866221 upstream gene variant T/C snv 0.10 12
rs931127
SIPA1 ; PCNX3
0.790 0.160 11 65637829 upstream gene variant G/A snv 0.49 12
rs1862513
RETN
0.763 0.360 19 7668907 upstream gene variant C/G;T snv 11
rs2486758
CYP17A1
0.742 0.160 10 102837723 upstream gene variant T/C snv 0.18 11
rs3754093
EXO1
0.776 0.240 1 241846814 upstream gene variant A/G snv 0.23 11
rs3758391
SIRT1
0.742 0.480 10 67883584 upstream gene variant T/C snv 0.64 11
rs2494752
AKT1
0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10
rs28366003
MT2A
0.763 0.240 16 56608579 upstream gene variant A/C;G snv 4.6E-02 10
rs2069514 0.807 0.160 15 74745879 upstream gene variant G/A snv 0.13 9
rs2119882
MTNR1A
0.807 0.320 4 186555751 upstream gene variant T/C snv 0.57 9
rs2073617
COLEC10 ; TNFRSF11B
0.776 0.360 8 118952044 upstream gene variant G/A snv 0.58 8
rs5743305
TLR3
0.807 0.200 4 186068179 upstream gene variant T/A snv 0.35 8
rs62514004
CCN4
0.790 0.240 8 133190246 upstream gene variant A/G snv 0.28 8
rs6498486
ERCC4
0.776 0.200 16 13919809 upstream gene variant A/C snv 0.27 8
rs2509049
H2AX
0.827 0.160 11 119095811 upstream gene variant C/A;T snv 6