Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1042489
BIRC5
0.851 0.160 17 78224125 3 prime UTR variant T/C snv 0.40 5
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1042636
CASR
0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 23
rs10426628
SULT2B1
0.925 0.080 19 48589173 intron variant A/G snv 0.78 2
rs10432782
SOD1
0.807 0.160 21 31664078 intron variant T/G snv 0.19 7
rs1045485
CASP8
0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs1045531
PSCA
0.882 0.080 8 142682129 synonymous variant C/A snv 0.45 0.44 3
rs10459592
CYP19A1 ; MIR4713HG
0.925 0.080 15 51243944 intron variant T/G snv 0.49 2
rs10460109 1.000 0.080 18 75324210 intergenic variant T/C snv 0.61 1
rs1046040
POLR2E
0.925 0.080 19 1095515 upstream gene variant G/A snv 0.21 2
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
rs1048169
HAUS6
1.000 0.080 9 19055967 3 prime UTR variant T/C snv 0.46 1
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