Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs937475913
PRKDC
0.790 0.120 8 47936435 missense variant T/C snv 4.0E-06 7
rs936554882
HOXB13
0.925 0.080 17 48726959 missense variant C/T snv 2.8E-05 2
rs9364554
SLC22A3
0.882 0.160 6 160412632 intron variant C/T snv 0.21 3
rs9350
EXO1
0.742 0.240 1 241885372 missense variant C/T snv 0.21 0.19 16
rs934737987
CDX2
0.925 0.080 13 27968862 missense variant C/T snv 7.0E-06 2
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs9332964
SRD5A2
0.763 0.240 2 31529325 missense variant C/T snv 4.7E-04 1.6E-04 10
rs9325782 0.851 0.120 8 16232964 intron variant C/T snv 0.87 6
rs9306895
GDF7
1.000 0.080 2 20678393 3 prime UTR variant T/C snv 0.29 1
rs9306412
CRYBB2
0.925 0.080 22 25225156 intron variant C/A snv 0.22 2
rs9296068 0.925 0.200 6 33020918 intergenic variant T/G snv 0.42 2
rs9287719
NOL10
1.000 0.080 2 10570604 downstream gene variant C/T snv 0.60 1
rs928554
ESR2
0.851 0.120 14 64227477 3 prime UTR variant C/T snv 0.66 6
rs9284813
LINC00506
0.925 0.080 3 87103019 intron variant A/G snv 0.22 2
rs9282858
SRD5A2
0.716 0.320 2 31580756 missense variant C/T snv 1.8E-02 2.1E-02 16
rs925013
LOC105372441
0.925 0.080 19 50850345 intron variant A/G;T snv 2
rs920778
HOTAIR
0.633 0.480 12 53966448 intron variant G/A snv 0.57 36
rs919467999
ERG
0.925 0.080 21 38383632 missense variant G/A snv 2
rs905883
ERBB4
0.851 0.120 2 212323745 intron variant C/G;T snv 6
rs902774 0.925 0.080 12 52880120 regulatory region variant G/A snv 0.12 2
rs895819
MIR23A ; LOC284454 ; MIR27A ; MIR24-2
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs895521
NPAS2
0.925 0.080 2 100935633 intron variant T/C snv 0.84 2
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs887391
PCAT19
0.925 0.080 19 41479716 intron variant T/C snv 0.31 2
rs887303970
SOD3
0.776 0.280 4 24799565 missense variant C/T snv 8.8E-06 7.0E-06 10