Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
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
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
rs67164370
RASSF2
0.851 0.120 20 4787830 intron variant -/AGGGACT ins 4
rs10098821
LINC00824
0.882 0.120 8 128546982 intron variant C/T snv 7.6E-02 3
rs11683487
NMI
0.882 0.120 2 151286035 intron variant G/T snv 0.36 3
rs13063604
RUVBL1
0.882 0.120 3 128085887 intron variant G/A snv 0.23 3
rs1516982
LINC00824
0.882 0.120 8 128521400 intron variant A/G snv 0.16 3
rs186724
AHCYL1
0.882 0.120 1 110018293 intron variant C/G;T snv 3
rs2153271
BNC2
0.925 0.160 9 16864523 intron variant C/T snv 0.43 3
rs2191249
BRIP1
0.882 0.120 17 61758503 intron variant T/G snv 0.79 3
rs2287497
WRAP53 ; TP53
0.882 0.120 17 7689462 intron variant G/A snv 0.25 3