Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9344
CCND1
0.653 0.480 11 69648142 splice region variant G/A snv 0.45 0.39 30
rs9341266
RMDN2 ; LOC107985872 ; CYP1B1
0.925 0.080 2 38068851 3 prime UTR variant G/A snv 3.8E-02 2
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs9332542
F5
0.925 0.080 1 169570045 intron variant G/A snv 0.27 3
rs9325782 0.851 0.120 8 16232964 intron variant C/T snv 0.87 6
rs932335
HSD11B1-AS1 ; HSD11B1
0.851 0.120 1 209732389 intron variant G/C snv 0.21 0.21 4
rs931127
SIPA1 ; PCNX3
0.790 0.160 11 65637829 upstream gene variant G/A snv 0.49 12
rs9306160
RRP1B
0.925 0.080 21 43687681 missense variant T/C snv 0.69 0.73 3
rs930395 0.925 0.080 5 44822356 upstream gene variant G/A;T snv 0.23 2
rs928940
IL1RN
0.882 0.120 2 113119918 intron variant G/T snv 0.78 3
rs9288518
XRCC5
0.776 0.240 2 216196997 intron variant A/G snv 0.35 9
rs928554
ESR2
0.851 0.120 14 64227477 3 prime UTR variant C/T snv 0.66 6
rs9282861
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 31
rs9282858
SRD5A2
0.716 0.320 2 31580756 missense variant C/T snv 1.8E-02 2.1E-02 10
rs927650
CYP24A1
0.763 0.240 20 54156202 intron variant T/A;C snv 9
rs926778
ESR1
0.925 0.080 6 152034647 intron variant C/A snv 0.40 2
rs9257809
OR12D3 ; OR5V1
0.790 0.320 6 29388554 intron variant A/G snv 5.8E-02 4
rs924038259
PPARGC1A
0.925 0.080 4 23828541 missense variant G/C snv 2
rs920778
HOTAIR
0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs919275
INSR
0.925 0.080 19 7261430 intron variant T/C snv 0.49 2
rs916537173
PDGFRA
0.925 0.080 4 54263784 missense variant A/G snv 2
rs915927
XRCC1
0.827 0.120 19 43553075 synonymous variant T/A;C;G snv 0.37 5
rs912505
CYP24A1
0.925 0.080 20 54160302 intron variant A/G;T snv 2
rs907187
PARP1
0.925 0.080 1 226407946 5 prime UTR variant C/G;T snv 0.21; 4.1E-06 2
rs906296
RUNX3 ; LOC105376878
0.925 0.080 1 24938167 intron variant C/G snv 0.76 2