Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4759314
HOTAIR
0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs2256787
ARHGEF10L
0.925 0.120 1 17566321 intron variant A/C snv 0.93 2
rs1192691 0.925 0.120 10 36880367 regulatory region variant G/T snv 0.90 2
rs1614627 1.000 0.120 1 20620263 downstream gene variant A/C snv 0.86 1
rs2660753 0.790 0.240 3 87061524 intergenic variant T/C snv 0.76 9
rs4286604 0.925 0.120 4 69576447 intron variant A/G snv 0.76 2
rs10017134
UGT2A2 ; UGT2A1
0.925 0.120 4 69591303 intron variant T/C snv 0.75 2
rs2252673
INSR
0.882 0.120 19 7150407 intron variant C/G snv 0.75 3
rs2803073
PRKN
0.925 0.120 6 162541796 intron variant G/A snv 0.74 2
rs851797
EXO1
0.752 0.240 1 241889740 3 prime UTR variant A/G snv 0.72 13
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65 10
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs7305032
VDR
0.925 0.120 12 47856077 intron variant G/A snv 0.61 2
rs10788679
ARHGEF10L
0.925 0.120 1 17590467 intron variant A/G snv 0.59 2
rs237028
TAB2
0.925 0.120 6 149397514 intron variant C/T snv 0.58 2
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs8044477 1.000 0.120 16 58942687 intron variant A/G snv 0.53 1
rs11651755
HNF1B
0.763 0.160 17 37739849 intron variant T/C snv 0.52 9
rs633862 0.925 0.120 9 133279871 upstream gene variant T/C snv 0.49 5
rs3834129
CASP8
0.627 0.560 2 201232809 upstream gene variant AGTAAG/- del 0.48 38
rs370681
AXIN1
0.807 0.200 16 342461 intron variant C/T snv 0.48 6
rs1017134 0.925 0.120 7 35307237 intergenic variant G/A snv 0.47 2
rs9283636 1.000 0.120 3 166315136 intergenic variant G/A snv 0.46 1
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157