Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs16917302
ZNF365
0.851 0.080 10 62501439 intron variant A/C snv 0.18 5
rs2296135
IL15RA
0.851 0.080 10 5952731 3 prime UTR variant A/C snv 0.58 5
rs267606841
GALNT3
0.882 0.120 2 165749801 missense variant A/C snv 5
rs779682021
CYP1A1
0.882 0.120 15 74721227 missense variant A/C snv 5
rs11895168
ERBB4
0.925 0.080 2 211377467 3 prime UTR variant A/C snv 0.68 4
rs1902023
UGT2B15
0.882 0.080 4 68670366 missense variant A/C snv 0.51 0.53 4
rs863225283
ALK
0.925 0.080 2 29213993 missense variant A/C snv 4
rs15869
BRCA2
0.925 0.080 13 32398875 3 prime UTR variant A/C snv 0.15 3
rs2231292
BCL2L10
1.000 0.040 15 52112665 missense variant A/C snv 0.41 0.48 3
rs1057519785
ALK
1.000 0.040 2 29222404 missense variant A/C snv 2
rs121918683
MYC ; CASC11
1.000 0.160 8 127738519 missense variant A/C snv 2
rs1367215622
PHLPP2
1.000 0.120 16 71714618 missense variant A/C snv 4.0E-06 2
rs748984440
VEGFA
1.000 0.040 6 43784546 stop lost A/C snv 4.0E-06 2
rs770251749
MLIP
1.000 0.120 6 54121506 missense variant A/C snv 4.0E-06 2
rs1057519820
MAP2K1
15 66436810 missense variant A/C snv 1
rs1304149814
PIK3CB
3 138699042 missense variant A/C snv 4.0E-06 1
rs13071247
CD80
3 119547946 intron variant A/C snv 0.14 1
rs2298735
LAMTOR3
4 99894460 upstream gene variant A/C snv 0.44 1
rs750626949
SNORA80D ; AIMP2
7 6015169 missense variant A/C snv 1.2E-05 1
rs779702949
HIF1A-AS3 ; HIF1A
14 61740887 missense variant A/C snv 4.0E-06 1
rs879148650
PRKAR1A
17 68527856 missense variant A/C snv 1
rs989692988
TP53
17 7676023 splice donor variant A/C snv 8.0E-06 1
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs78311289
FGFR3
0.689 0.440 4 1806162 missense variant A/C;G snv 4.0E-06 25
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv 23