Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs585224 0.925 0.080 12 52529088 regulatory region variant A/G snv 0.66 0.50 2
rs41115
APC
0.882 0.160 5 112840073 synonymous variant G/A snv 0.65 0.59 3
rs2705897
CASP3
0.925 0.080 4 184631944 splice region variant T/G snv 0.64 0.73 4
rs2394882
POU5F1 ; TCF19
0.882 0.080 6 31164872 splice region variant A/C snv 0.64 0.69 3
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs7813
GEMIN4
0.689 0.360 17 744946 missense variant G/A;C snv 0.63 22
rs1058808
ERBB2
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs746924
TBC1D8 ; RPL31
0.925 0.080 2 101008009 missense variant T/C snv 0.61 0.61 2
rs238406
ERCC2
0.677 0.480 19 45365051 synonymous variant T/G snv 0.58 0.65 23
rs605059
HSD17B1 ; LOC108783654
0.763 0.160 17 42554888 missense variant G/A;C;T snv 0.56; 9.0E-05; 1.4E-05 15
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs4148269
UGT2B15
0.882 0.080 4 68647129 missense variant T/G snv 0.55 0.49 3
rs7121
GNAS
0.882 0.160 20 58903752 missense variant C/G;T snv 0.54 6
rs627928
RNASEL
0.790 0.080 1 182582202 missense variant A/C snv 0.54 0.49 10
rs1052576
CASP9
0.807 0.200 1 15506048 missense variant T/A;C snv 0.53 9
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs6923492
GRM1
0.925 0.080 6 146434188 missense variant T/C snv 0.52 0.57 2
rs1047768
ERCC5 ; BIVM-ERCC5
0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs208294
P2RX7 ; LOC105370032
0.790 0.320 12 121162450 missense variant T/A;C;G snv 0.51 9
rs1902023
UGT2B15
0.882 0.080 4 68670366 missense variant A/C snv 0.51 0.53 4
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs12529
AKR1C3
0.776 0.280 10 5094459 missense variant C/G snv 0.50 0.45 10
rs2494732
AKT1
0.763 0.240 14 104772855 intron variant T/C snv 0.50 0.47 11
rs4880
SOD2
0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131