Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs56404467
FRY
0.708 0.280 13 32265853 intron variant G/A snv 1.3E-02 17
rs73110464
KRT8
0.708 0.280 12 52918828 intron variant C/T snv 0.12 17
rs7725218
TERT
0.708 0.280 5 1282299 intron variant G/A snv 0.38 17
rs1271572
ESR2
0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs2107425
MRPL23 ; H19
0.732 0.280 11 1999845 intron variant C/T snv 16
rs7705526
TERT
0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs11954856
APC
0.732 0.200 5 112751630 intron variant T/G snv 0.54 12
rs2494938
LRFN2
0.752 0.240 6 40568389 intron variant G/A snv 0.51 11
rs2699887
PIK3CA ; LOC101928739
0.763 0.280 3 179148620 intron variant C/T snv 0.18 11
rs11651755
HNF1B
0.763 0.160 17 37739849 intron variant T/C snv 0.52 9
rs4648068
NFKB1
0.790 0.240 4 102597148 intron variant A/G snv 0.31 9
rs11655505
NBR2 ; BRCA1
0.776 0.160 17 43126360 intron variant G/A snv 0.31 8
rs1989839
ZMYND10 ; RASSF1
0.790 0.160 3 50341515 intron variant A/G snv 0.22 0.20 8
rs2665390
LOC107986148 ; TIPARP
0.776 0.160 3 156679960 intron variant C/T snv 0.92 8
rs1243180
MLLT10
0.790 0.160 10 21626690 intron variant T/A snv 0.23 7
rs1469713
GATAD2A
0.827 0.160 19 19417997 intron variant A/G snv 0.44 7
rs7937840
INCENP
0.807 0.200 11 62126500 intron variant C/T snv 0.20 7
rs2708861
HUS1
0.851 0.120 7 47977120 intron variant T/G snv 0.46 6
rs4533622
CTNNB1
0.807 0.240 3 41200847 intron variant C/A;T snv 6
rs5013329
NSUN4
0.827 0.160 1 46349419 intron variant C/T snv 0.23 6
rs7405776
HNF1B
0.807 0.120 17 37733029 intron variant G/A;C snv 6
rs757210
HNF1B
0.807 0.160 17 37736525 intron variant C/G;T snv 6
rs9375701
L3MBTL3
0.827 0.160 6 130062912 intron variant C/T snv 0.53 6
rs12373237
LAMA3
0.851 0.200 18 23845972 intron variant G/A snv 0.47 5
rs3923087
AXIN2
0.827 0.160 17 65553143 intron variant T/C snv 0.58 5