Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2299939
PTEN
0.827 0.080 10 87897393 intron variant C/A;T snv 5
rs12334811
PRKDC
0.851 0.080 8 47920417 intron variant G/A snv 0.15 4
rs75790006 0.851 0.040 4 43211547 intron variant T/G snv 1.1E-02 4
rs8178085
PRKDC
0.851 0.080 8 47898144 intron variant T/G snv 2.3E-02 4
rs12934561
IL32
0.882 0.080 16 3068864 intron variant T/C snv 0.57 3
rs1340420
TNKS2
0.925 0.080 10 91857549 intron variant A/G snv 0.71 0.70 3
rs1770474
TNKS2
0.925 0.080 10 91833770 intron variant G/A;T snv 3
rs181696
PLCH1
0.925 0.080 3 155548315 intron variant T/C snv 0.55 3
rs2847281
PTPN2
1.000 0.040 18 12821594 intron variant A/G snv 0.32 3
rs4268748
DEF8
0.925 0.080 16 89960104 intron variant T/C snv 0.30 3
rs471692
TOP2A
0.925 0.080 17 40400518 intron variant T/A;C snv 0.79 3
rs4822983
CHEK2
0.925 0.080 22 28719078 intron variant C/T snv 0.33 3
rs1670661
NELL1
1.000 0.040 11 21209124 intron variant C/G;T snv 2
rs17761864
SMG6
1.000 0.040 17 2268343 intron variant C/A snv 0.28 2
rs2239612
ST6GAL1
1.000 0.040 3 187075454 intron variant G/A snv 0.17 2
rs4785204
HEATR3
1.000 0.040 16 50069823 intron variant C/T snv 8.6E-02 2
rs6819385
CHRNA9
0.925 0.080 4 40337557 intron variant A/G snv 0.52 2
rs7182283
NEIL1
0.925 0.120 15 75351418 intron variant G/T snv 0.43 2
rs754626
SRC
0.925 0.080 20 37388937 intron variant T/G snv 0.25 2
rs1078305
GSN
1.000 0.040 9 121289122 intron variant A/G snv 0.70 1
rs10818524
GSN
1.000 0.040 9 121267901 intron variant T/C snv 0.37 1
rs11707807
LPP
1.000 0.040 3 188370473 intron variant A/G snv 0.36 1
rs117984432
ANKRD11
1.000 0.040 16 89388583 intron variant T/C snv 2.0E-02 1
rs13301660
SEC16A
1.000 0.040 9 136446350 intron variant C/T snv 0.20 1
rs1460816
BRCA2
1.000 0.040 13 32354271 intron variant G/A snv 0.54 1