Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs387906661
BRAF
0.807 0.280 7 140801551 missense variant T/G snv 6
rs11778573
CCN4
0.851 0.080 8 133216687 intron variant T/G snv 0.59 4
rs12674822
MCPH1 ; ANGPT2
0.851 0.200 8 6531695 intron variant T/G snv 0.49 4
rs8178085
PRKDC
0.851 0.080 8 47898144 intron variant T/G snv 2.3E-02 4
rs2562796
HIBCH
0.882 0.080 2 190248283 intron variant T/G snv 0.30 3
rs3212980
ERCC1
0.882 0.080 19 45413183 intron variant T/G snv 0.26 3
rs4246444
FASN
0.882 0.080 17 82081076 intron variant T/G snv 0.75 3
rs1419255508
MXRA5
1.000 0.080 X 3310056 missense variant T/G snv 9.6E-06 1
rs17181550
LINC00511
1.000 0.080 17 72303817 intron variant T/G snv 0.38 1
rs2741348
EPHX2 ; GULOP
1.000 0.080 8 27563265 intron variant T/G snv 0.50 1
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs886039484
TP53
0.641 0.440 17 7674888 missense variant T/C;G snv 32
rs1800440
CYP1B1
0.653 0.440 2 38070996 missense variant T/C;G snv 0.15; 4.0E-06 29
rs1760944
OSGEP ; APEX1
0.672 0.480 14 20454990 non coding transcript exon variant T/C;G snv 26
rs6721961
NFE2L2
0.672 0.520 2 177265309 intron variant T/C;G snv 0.89 24
rs1800975
XPA
0.701 0.360 9 97697296 5 prime UTR variant T/C;G snv 0.63; 4.5E-06; 4.5E-06 19
rs1202989817
SOD1 ; LOC102724449
0.716 0.360 21 31659813 missense variant T/C;G snv 8.0E-06 7.0E-06 18
rs652438
MMP12
0.716 0.400 11 102865911 missense variant T/C;G snv 7.1E-02; 2.5E-04 14
rs770460061
GSTP1
0.742 0.240 11 67585239 missense variant T/C;G snv 4.0E-06; 1.2E-05 14
rs2227284
IL4
0.732 0.480 5 132677033 intron variant T/C;G snv 12
rs7025417
LOC107987046 ; IL33
0.752 0.280 9 6240084 intron variant T/C;G snv 11
rs376040996
XPA
0.790 0.120 9 97687210 missense variant T/C;G snv 1.2E-05; 2.0E-05 7
rs884225
EGFR
0.827 0.160 7 55206391 3 prime UTR variant T/C;G snv 5
rs11072768
CHRNB4
0.882 0.080 15 78637136 intron variant T/C;G snv 4
rs200100285
MTHFR
0.851 0.080 1 11796313 missense variant T/C;G snv 1.9E-04 4