Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9913017
SLC39A11
0.882 0.120 17 73014881 intron variant A/C;T snv 3
rs9904341
BIRC5
0.695 0.280 17 78214286 5 prime UTR variant G/A;C;T snv 0.38; 4.8E-06 20
rs9642880
CASC11
0.776 0.240 8 127705823 intron variant G/A;T snv 9
rs9624880
GRK3
0.882 0.120 22 25588025 intron variant C/T snv 3
rs9619311
TIMP3 ; SYN3
0.851 0.160 22 32800707 intron variant T/C snv 0.40 4
rs953038635
SOD2
0.590 0.800 6 159692720 missense variant G/A;T snv 8.0E-06 51
rs937475913
PRKDC
0.790 0.120 8 47936435 missense variant T/C snv 4.0E-06 7
rs9297976
JRK ; PSCA
0.790 0.160 8 142670817 intron variant T/C;G snv 7
rs9288518
XRCC5
0.776 0.240 2 216196997 intron variant A/G snv 0.35 9
rs9282861
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 31
rs921142 0.882 0.120 8 41311757 upstream gene variant T/C snv 0.31 3
rs9034
NAMPT
0.827 0.200 7 106249610 3 prime UTR variant A/G;T snv 5
rs887569
EZH2
0.882 0.120 7 148808210 intron variant C/T snv 0.73 5
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs874945 0.732 0.240 12 53961667 upstream gene variant C/T snv 0.38 14
rs8679
PARP1
0.790 0.200 1 226360853 3 prime UTR variant A/G snv 0.16 7
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs861531
XRCC3 ; LOC112268131 ; KLC1
0.882 0.120 14 103706470 3 prime UTR variant C/A snv 0.32 3
rs861530
LOC112268131 ; XRCC3 ; KLC1
0.732 0.320 14 103707786 3 prime UTR variant T/C snv 0.65 13
rs8444
CERS2
0.882 0.120 1 150966095 3 prime UTR variant G/A snv 0.35 3
rs833052 0.827 0.160 6 43755598 intergenic variant A/C snv 0.88 5
rs8179090
TIMP2
0.752 0.280 17 78925807 upstream gene variant C/G snv 1.6E-02 12
rs8102137 0.882 0.120 19 29805946 regulatory region variant T/C snv 0.24 3
rs8041357
ARID3B
0.882 0.120 15 74577097 intron variant T/C snv 6.6E-02 3
rs80357138
BRCA1
0.763 0.200 17 43094776 missense variant C/T snv 8.0E-06 9