Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1047303
HSD3B1
0.851 0.120 1 119514623 missense variant C/A snv 0.75 4
rs1047768
ERCC5 ; BIVM-ERCC5
0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs1047840
EXO1
0.708 0.280 1 241878999 missense variant G/A snv 0.36 0.40 19
rs10483813
RAD51B
0.851 0.120 14 68564567 intron variant T/A;C snv 4
rs10486567
JAZF1
0.851 0.120 7 27936944 intron variant G/A snv 0.28 9
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs1049216
CASP3
0.790 0.200 4 184628935 3 prime UTR variant A/G snv 0.27 9
rs10503733
LOC107986930
0.925 0.080 8 23676505 downstream gene variant G/T snv 0.27 2
rs1050450
GPX1
0.623 0.600 3 49357401 missense variant G/A snv 0.28 0.30 43
rs10505346
COLEC10 ; TNFRSF11B
0.925 0.080 8 118951604 intron variant G/T snv 0.22 4
rs10505474
CASC8 ; PCAT1 ; POU5F1B
0.925 0.080 8 127405259 intron variant T/C snv 0.47 3
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs10505483
PCAT1 ; CASC19
0.925 0.080 8 127112950 intron variant C/T snv 0.16 2
rs10519097
RORA
0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1052576
CASP9
0.807 0.200 1 15506048 missense variant T/A;C snv 0.53 9
rs1056827
CYP1B1 ; CYP1B1-AS1
0.683 0.400 2 38075034 missense variant C/A snv 0.32 0.35 24
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1057519864
AR
0.851 0.080 X 67723707 missense variant T/C snv 8
rs1057519912
MED12
0.776 0.200 X 71129408 missense variant C/G;T snv 11
rs1057519966
LOC107984999 ; SPOP
0.882 0.080 17 49619064 missense variant A/C;T snv 3
rs1057519972
SPOP ; LOC107984999
0.882 0.080 17 49619327 missense variant A/T snv 3
rs1057520005
TP53
0.742 0.360 17 7673800 missense variant C/A;G snv 14
rs1058205
KLK3
0.925 0.080 19 50860142 3 prime UTR variant C/T snv 0.75 0.74 3
rs1058587
GDF15
0.882 0.200 19 18388612 missense variant C/G;T snv 0.24; 9.1E-06 4