Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4733613 1.000 0.080 8 128587032 intergenic variant C/G snv 0.86 1
rs2494750
AKT1
0.925 0.080 14 104796575 upstream gene variant G/C snv 0.86 2
rs12184995
LINC02331 ; LOC105370504
1.000 0.080 14 53759970 intron variant A/G snv 0.83 1
rs1801132
ESR1
0.689 0.320 6 151944387 synonymous variant G/C snv 0.73 0.80 22
rs1923357
PTPRD
1.000 0.080 9 10266786 intron variant C/T snv 0.72 1
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs34330
CDKN1B ; GPR19
0.724 0.280 12 12717761 5 prime UTR variant T/C snv 0.70 15
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 14
rs2414098
CYP19A1 ; MIR4713HG
1.000 0.080 15 51245609 intron variant T/C snv 0.65 2
rs757211
HNF1B
1.000 0.080 17 37736488 intron variant T/C snv 0.65 1
rs238406
ERCC2
0.677 0.480 19 45365051 synonymous variant T/G snv 0.58 0.65 23
rs4851527
IL1R2
0.790 0.160 2 102005914 intron variant A/G snv 0.63 7
rs1337082
LOC105373241
0.925 0.080 X 67764173 intergenic variant G/A snv 0.61 2
rs2960422
PPARG
1.000 0.080 3 12293492 intron variant G/A snv 0.59 2
rs17601876
MIR4713HG ; CYP19A1
1.000 0.080 15 51261712 intron variant A/G snv 0.58 3
rs12934561
IL32
0.882 0.080 16 3068864 intron variant T/C snv 0.57 3
rs752760
CYP19A1
0.925 0.080 15 51339282 upstream gene variant C/T snv 0.57 2
rs9668337
LOC105369704 ; LOC105369705 ; SSPN
1.000 0.080 12 26273405 non coding transcript exon variant G/A snv 0.55 1
rs4052756 1.000 0.080 6 19914263 intergenic variant C/T snv 0.55 1
rs2278868
SKAP1
0.925 0.080 17 48184809 missense variant C/T snv 4.0E-06; 0.63 0.55 2
rs7579014
BCL11A
1.000 0.080 2 60480759 intron variant G/A snv 0.55 2
rs1740828 0.925 0.080 6 21648854 regulatory region variant G/A snv 0.55 2
rs11651755
HNF1B
0.763 0.160 17 37739849 intron variant T/C snv 0.52 9
rs882380
SKAP1
1.000 0.080 17 48216874 intron variant C/A snv 0.52 1