Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs10821936
ARID5B
0.742 0.200 10 61963818 intron variant C/T snv 0.69 11
rs3116496
CD28
0.776 0.160 2 203729789 intron variant T/C snv 0.15 0.14 11
rs2293157
STAT5A
0.763 0.120 17 42300657 intron variant C/A;T snv 9
rs10740055
ARID5B
0.790 0.240 10 61958720 intron variant C/A snv 0.49 7
rs2413739
PACSIN2
0.827 0.120 22 43001030 intron variant C/T snv 0.43 6
rs10251201
UMAD1
0.851 0.160 7 7932654 intron variant T/A;C snv 4
rs11079041
STAT5B
0.882 0.040 17 42262061 intron variant T/A;C snv 0.36 4
rs974120 0.851 0.200 8 2789080 intron variant T/C;G snv 4
rs10405859
PPP1R37 ; MARK4
0.882 0.080 19 45099523 intron variant T/C snv 0.48 3
rs6964823
IKZF1
0.925 0.040 7 50392398 intron variant G/A snv 0.45 3
rs9318227
KLF12
0.882 0.080 13 73926833 intron variant T/A;C snv 3
rs10931910
AOX1
0.925 0.040 2 200659013 intron variant A/G;T snv 2
rs17886724
STAT3
0.925 0.040 17 42344145 intron variant A/G snv 0.35 2
rs7090445
ARID5B
0.925 0.120 10 61961417 intron variant C/G;T snv 0.70 2
rs10065633
IRF1-AS1
1.000 0.040 5 132481024 intron variant T/C snv 0.38 1
rs113017087
APC
1.000 0.040 5 112737780 intron variant T/C snv 5.4E-03 1
rs75612255
APC
1.000 0.040 5 112737543 intron variant T/C snv 1
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs562015640
PTEN
0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 16
rs387906659
AKT2
0.742 0.280 19 40257052 stop gained C/A;T snv 14
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480