Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs230496
NFKB1
0.882 0.080 4 102567334 intron variant G/A snv 0.59 3
rs16901979
PCAT1 ; CASC19
0.724 0.480 8 127112671 intron variant C/A snv 0.16 17
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs3811741
PLK4
0.882 0.080 4 127882004 intron variant G/A snv 0.74 3
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs2299939
PTEN
0.827 0.080 10 87897393 intron variant C/A;T snv 5
rs1234220
PTEN
0.851 0.080 10 87885716 intron variant A/G snv 9.1E-02 4
rs745501336
RAB43 ; ISY1-RAB43
0.882 0.080 3 129091263 missense variant C/T snv 4.6E-05 7.0E-06 3
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 37
rs2296651
SLC10A1
0.732 0.240 14 69778476 missense variant G/A snv 6.3E-03 2.5E-03 13
rs769031989
STAT3
0.851 0.160 17 42322464 missense variant T/A snv 7.0E-06 4
rs2853669
TERT
0.649 0.320 5 1295234 upstream gene variant A/G snv 0.25 35
rs2241715
TGFB1
0.851 0.120 19 41350981 5 prime UTR variant A/C snv 0.68 4
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs20576
TNFRSF10A
0.637 0.400 8 23200707 missense variant T/G snv 0.15 0.14 34
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs121912666
TP53
0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 34
rs28934571
TP53
0.645 0.360 17 7674216 missense variant C/A;G snv 31
rs587782237
TP53
0.882 0.080 17 7670637 missense variant C/T snv 3
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs3734091
XRCC4
0.689 0.280 5 83204915 missense variant G/T snv 2.3E-02 1.4E-02 19
rs80309960
XRCC5
0.851 0.080 2 216122110 missense variant T/A snv 3.5E-04 1.1E-03 4