Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2736098
TERT
0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs2853677
TERT
0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 19
rs10993994
MSMB
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54 15
rs4430796
HNF1B
0.790 0.280 17 37738049 intron variant A/G snv 0.52 14
rs7501939
HNF1B
0.776 0.280 17 37741165 intron variant C/T snv 0.41 12
rs10486567
JAZF1
0.851 0.120 7 27936944 intron variant G/A snv 0.28 9
rs2735839 0.827 0.160 19 50861367 upstream gene variant A/C;G snv 7
rs11651052
HNF1B
0.851 0.200 17 37742390 intron variant G/A snv 0.50 7
rs2900333
ATF7IP
0.882 0.200 12 14500933 3 prime UTR variant C/A;G;T snv 6
rs17632542
KLK3
0.925 0.080 19 50858501 missense variant T/C snv 5.5E-02 4.9E-02 5
rs266849
LOC105372441
0.925 0.080 19 50845834 intron variant G/A snv 0.82 4
rs1991431
ZBTB38
3 141414608 intron variant G/A snv 0.50 4
rs11067228 0.925 0.080 12 114656455 downstream gene variant A/G snv 0.37 3
rs11084596 1.000 0.040 19 31614073 regulatory region variant T/C snv 0.35 3
rs11199879 1.000 0.040 10 121285698 regulatory region variant T/C snv 0.18 3
rs4631830 0.925 0.080 10 46052478 upstream gene variant A/G snv 0.43 3
rs11055980
ATF7IP
1.000 0.040 12 14458588 intron variant C/T snv 0.40 3
rs3213764
ATF7IP
0.925 0.080 12 14434367 missense variant A/G snv 0.47 0.42 3
rs2556378
BCL11A
1.000 0.040 2 60535367 3 prime UTR variant T/G snv 0.81 3
rs381949
CLPTM1L
1.000 0.040 5 1322353 intron variant G/A snv 0.44 3
rs3744763
HNF1B
0.925 0.160 17 37730894 non coding transcript exon variant A/G snv 0.30 3
rs1058205
KLK3
0.925 0.080 19 50860142 3 prime UTR variant C/T snv 0.75 0.74 3
rs61752561
KLK3
0.925 0.080 19 50858126 missense variant G/A snv 2.4E-02 2.5E-02 3