Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9282861
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 31
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
rs33931746
HBB
0.807 0.280 11 5227099 5 prime UTR variant T/C;G snv 6
rs35518301
HBD
0.827 0.200 11 5234514 5 prime UTR variant T/C snv 6
rs137852576
AR
0.827 0.240 X 67686067 missense variant G/A snv 5
rs183433761
GCG ; LOC101929532
0.851 0.200 2 162152278 5 prime UTR variant T/C;G snv 5
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
rs34500389
HBB
0.851 0.280 11 5227103 5 prime UTR variant G/A;T snv 4
rs202155613
BRCA2
0.882 0.200 13 32379902 stop gained C/A;G;T snv 4.0E-05 3
rs397509430
HBB
0.882 0.200 11 5227101 5 prime UTR variant A/- del 3
rs786203411
BRCA2
0.925 0.120 13 32398582 missense variant A/G snv 7.0E-06 2
rs281864525
HBB
0.851 0.280 11 5227097 5 prime UTR variant T/A;G snv 7.0E-06 4
rs63750953
HBB
0.790 0.400 11 5227097 5 prime UTR variant TT/- delins 7.0E-06 10
rs34166473
HBD
0.827 0.320 11 5234513 5 prime UTR variant A/G snv 7.0E-06 6
rs562962093
MBL2
0.742 0.520 10 52771740 upstream gene variant T/C snv 7.0E-06 13
rs200487063
LEP
0.851 0.200 7 128241246 upstream gene variant G/A snv 2.1E-05 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
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
rs72661131
MBL2
0.742 0.480 10 52771739 upstream gene variant A/G snv 7.6E-04 15
rs34598529
HBB
0.724 0.280 11 5227100 5 prime UTR variant T/C snv 8.9E-04 14
rs35036378
ESR2
0.851 0.200 14 64294403 5 prime UTR variant A/C snv 7.0E-03 5