Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs17401966
KIF1B
0.790 0.280 1 10325413 intron variant A/G snv 0.24 7
rs7937840
INCENP
0.807 0.200 11 62126500 intron variant C/T snv 0.20 7
rs1256030
ESR2
0.827 0.240 14 64280452 intron variant A/G;T snv 6
rs2708861
HUS1
0.851 0.120 7 47977120 intron variant T/G snv 0.46 6
rs370681
AXIN1
0.807 0.200 16 342461 intron variant C/T snv 0.48 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
rs638820
GSTM4 ; GSTM2
0.827 0.160 1 109667284 intron variant G/A snv 0.52 5
rs10088218
LINC00824
0.851 0.120 8 128531703 intron variant G/A snv 0.13 4
rs11084033
LOC105372441
0.882 0.120 19 50850699 intron variant C/A;T snv 4
rs11782652
CHMP4C
0.851 0.120 8 81741409 intron variant A/G snv 6.6E-02 4
rs185229225
BOD1L1
0.851 0.120 4 13607505 intron variant T/C snv 4
rs230521
NFKB1
0.851 0.160 4 102542171 intron variant C/G snv 0.59 4
rs495139
ENOSF1
0.882 0.120 18 676008 intron variant G/C snv 0.63 4
rs4988344
BRIP1
0.882 0.120 17 61847251 intron variant G/C snv 0.20 0.15 4