Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10941679 0.763 0.120 5 44706396 intergenic variant A/G snv 0.25 11
rs6504950
STXBP4
0.807 0.120 17 54979110 intron variant G/A snv 0.29 7
rs1314913
RAD51B
0.807 0.120 14 68232877 intron variant C/T snv 0.13 6
rs55971303
BRCA1
0.851 0.120 17 43104138 missense variant G/T snv 1.0E-04 4.2E-05 4
rs786203411
BRCA2
0.925 0.120 13 32398582 missense variant A/G snv 7.0E-06 2
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
rs2588809
RAD51B
0.807 0.160 14 68193711 intron variant T/C snv 0.80 6
rs9383938
ESR1
0.827 0.160 6 151666222 intron variant G/T snv 0.11 5
rs999737
RAD51B
0.776 0.200 14 68567965 intron variant C/T snv 0.16 8
rs35518301
HBD
0.827 0.200 11 5234514 5 prime UTR variant T/C snv 6
rs183433761
GCG ; LOC101929532
0.851 0.200 2 162152278 5 prime UTR variant T/C;G snv 5
rs200487063
LEP
0.851 0.200 7 128241246 upstream gene variant G/A snv 2.1E-05 5
rs201739205
LOC108783654 ; HSD17B1
0.851 0.200 17 42552898 5 prime UTR variant A/C snv 7.8E-03 8.2E-03 5
rs34104384
LEP
0.851 0.200 7 128241254 upstream gene variant A/T snv 8.2E-03 5
rs35036378
ESR2
0.851 0.200 14 64294403 5 prime UTR variant A/C snv 7.0E-03 5
rs56187033
BRCA1
0.851 0.200 17 43099786 missense variant T/C snv 2.6E-04 2.9E-04 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
rs10895068
PGR ; PGR-AS1
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02 14
rs137852576
AR
0.827 0.240 X 67686067 missense variant G/A snv 5
rs2046210 0.708 0.280 6 151627231 intergenic variant G/A snv 0.41 21
rs13387042
LOC105373874 ; LOC101928278
0.732 0.280 2 217041109 intergenic variant A/G snv 0.44 16
rs34598529
HBB
0.724 0.280 11 5227100 5 prime UTR variant T/C snv 8.9E-04 14
rs2981579
FGFR2
0.776 0.280 10 121577821 intron variant A/G snv 0.53 8
rs137852573
AR
0.807 0.280 X 67686064 missense variant G/A snv 6