Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1360698171
RNASEL
0.851 0.080 1 182584103 missense variant T/C snv 4
rs149709822
KLK3
0.882 0.080 19 50856335 missense variant G/A snv 4.0E-05 2.3E-04 4
rs17036508
MTOR ; ANGPTL7
0.925 0.080 1 11195977 3 prime UTR variant T/C snv 9.0E-02 4
rs17309872
ACSS2 ; GSS
0.925 0.080 20 34927985 downstream gene variant A/C;G;T snv 4
rs188140481
PCAT1 ; CASC19
0.925 0.080 8 127179427 non coding transcript exon variant T/A;C snv 4
rs1902023
UGT2B15
0.882 0.080 4 68670366 missense variant A/C snv 0.51 0.53 4
rs1983891
FOXP4
0.925 0.080 6 41568689 intron variant C/T snv 0.35 4
rs198977
KLK2
0.925 0.080 19 50878521 missense variant C/T snv 0.24 0.30 4
rs266849
LOC105372441
0.925 0.080 19 50845834 intron variant G/A snv 0.82 4
rs266882
KLK3
0.925 0.080 19 50854757 upstream gene variant G/A snv 0.49 4
rs2705897
CASP3
0.925 0.080 4 184631944 splice region variant T/G snv 0.64 0.73 4
rs339331
RFX6
0.882 0.080 6 116888889 intron variant T/C snv 0.28 4
rs367590266
GSTA1
0.925 0.080 6 52797630 missense variant T/C snv 1.2E-05 7.0E-06 4
rs368952331
CYP1A1
0.925 0.080 15 74722805 missense variant C/T snv 2.8E-05 6.3E-05 4
rs4647603
PRIMPOL ; CASP3
0.925 0.080 4 184648576 5 prime UTR variant C/T snv 0.11 4
rs544190
PCA3 ; PRUNE2
0.851 0.080 9 76763591 intron variant G/A snv 0.32 4
rs6020712
CTNNBL1
1.000 0.080 20 37758210 intron variant G/A snv 0.12 4
rs6763931
ZBTB38
0.925 0.080 3 141383991 intron variant G/A snv 0.54 4
rs6983269 0.925 0.080 8 2741967 intron variant C/A;G;T snv 0.42 4
rs765521022
KLK3
0.851 0.080 19 50858171 missense variant T/C snv 4
rs772893086
ADARB1
0.925 0.080 21 45176099 missense variant A/C;G;T snv 4.0E-06 4
rs775220785
CYP3A4
0.925 0.080 7 99772615 missense variant C/T snv 8.0E-06 4
rs780354238
POLB
0.925 0.080 8 42369855 missense variant A/G snv 4.4E-06 4
rs822391
ADIPOQ
0.925 0.080 3 186846014 intron variant C/T snv 0.85 4
rs1045531
PSCA
0.882 0.080 8 142682129 synonymous variant C/A snv 0.45 0.44 3