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
rs243865
MMP2
0.600 0.640 16 55477894 intron variant C/T snv 0.19 48
rs7804372
CAV1
0.716 0.320 7 116554174 intron variant T/A snv 0.27 19
rs28360071
XRCC4
0.708 0.240 5 83142293 intron variant GATGAGGAAACTAACTCTCAGTGGTGTTTA/- delins 0.48 18
rs6869366
XRCC4 ; TMEM167A
0.701 0.280 5 83075927 intron variant T/G snv 9.2E-02 18
rs3807987
CAV1
0.732 0.280 7 116539780 intron variant G/A snv 7.6E-02 17
rs2285053
MMP2
0.752 0.320 16 55478465 intron variant C/T snv 0.12 15
rs28360317
XRCC4
0.716 0.280 5 83323739 intron variant -/CCT delins 0.24 15
rs2075685
TMEM167A ; XRCC4
0.724 0.320 5 83076846 intron variant G/A;T snv 14
rs2075686
TMEM167A ; XRCC4
0.742 0.240 5 83076927 intron variant C/T snv 1.7E-02 13
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
rs7727691
XRCC4 ; TMEM167A
0.763 0.200 5 83075876 intron variant C/T snv 0.32 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
rs3807992
CAV1
0.925 0.080 7 116557191 intron variant G/A snv 0.28 5
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
rs12672038
CAV1
0.925 0.080 7 116547052 intron variant G/A snv 7.6E-02 4
rs3757733
CAV1
1.000 0.040 7 116553675 intron variant T/A snv 0.26 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
rs227060
C11orf65 ; ATM
0.882 0.160 11 108334154 intron variant C/T snv 0.27 3