Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs10941679 0.763 0.120 5 44706396 intergenic variant A/G snv 0.25 11
rs137852593
AR
0.827 0.160 X 67717484 missense variant G/A;C;T snv 2.2E-05; 1.1E-05; 9.1E-04 8
rs137852573
AR
0.807 0.280 X 67686064 missense variant G/A snv 6
rs137852576
AR
0.827 0.240 X 67686067 missense variant G/A snv 5
rs55971303
BRCA1
0.851 0.120 17 43104138 missense variant G/T snv 1.0E-04 4.2E-05 4
rs56187033
BRCA1
0.851 0.200 17 43099786 missense variant T/C snv 2.6E-04 2.9E-04 4
rs144848
BRCA2
0.653 0.440 13 32332592 missense variant A/C snv 0.28 0.23 29
rs202155613
BRCA2
0.882 0.200 13 32379902 stop gained C/A;G;T snv 4.0E-05 3
rs786203411
BRCA2
0.925 0.120 13 32398582 missense variant A/G snv 7.0E-06 2
rs3803662
CASC16
0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs9383938
ESR1
0.827 0.160 6 151666222 intron variant G/T snv 0.11 5
rs35036378
ESR2
0.851 0.200 14 64294403 5 prime UTR variant A/C snv 7.0E-03 5
rs549591993
F7
0.776 0.400 13 113105794 5 prime UTR variant C/A snv 4.0E-04 2.8E-05 12
rs367732974
F7
0.790 0.360 13 113105788 5 prime UTR variant G/A snv 8.9E-05 2.8E-05 9
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58 21
rs2981579
FGFR2
0.776 0.280 10 121577821 intron variant A/G snv 0.53 8
rs183433761
GCG ; LOC101929532
0.851 0.200 2 162152278 5 prime UTR variant T/C;G snv 5
rs34598529
HBB
0.724 0.280 11 5227100 5 prime UTR variant T/C snv 8.9E-04 14
rs63750953
HBB
0.790 0.400 11 5227097 5 prime UTR variant TT/- delins 7.0E-06 10
rs33931746
HBB
0.807 0.280 11 5227099 5 prime UTR variant T/C;G snv 6
rs33980857
HBB
0.827 0.280 11 5227101 5 prime UTR variant A/C;G;T snv 5
rs33981098
HBB
0.827 0.280 11 5227102 5 prime UTR variant T/C;G snv 5
rs281864525
HBB
0.851 0.280 11 5227097 5 prime UTR variant T/A;G snv 7.0E-06 4
rs34500389
HBB
0.851 0.280 11 5227103 5 prime UTR variant G/A;T snv 4