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
rs2665390
LOC107986148 ; TIPARP
0.776 0.160 3 156679960 intron variant C/T snv 0.92 8
rs1192691 0.925 0.120 10 36880367 regulatory region variant G/T snv 0.90 2
rs1950902
MTHFD1
0.776 0.240 14 64415662 missense variant A/G snv 0.83 0.83 11
rs2227564
PLAU ; C10orf55
0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 15
rs2191249
BRIP1
0.882 0.120 17 61758503 intron variant T/G snv 0.79 3
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
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2228001
XPC
0.570 0.480 3 14145949 missense variant G/T snv 0.63 0.65 60
rs238406
ERCC2
0.677 0.480 19 45365051 synonymous variant T/G snv 0.58 0.65 23
rs314276
LIN28B
0.807 0.280 6 104960124 intron variant A/C snv 0.65 10
rs3803662
CASC16
0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs495139
ENOSF1
0.882 0.120 18 676008 intron variant G/C snv 0.63 4
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs1467465
THEMIS2
0.827 0.160 1 27884892 non coding transcript exon variant A/G snv 0.61 7
rs7305032
VDR
0.925 0.120 12 47856077 intron variant G/A snv 0.61 2
rs351771
APC
0.882 0.120 5 112828864 synonymous variant G/A snv 0.65 0.59 3
rs10788679
ARHGEF10L
0.925 0.120 1 17590467 intron variant A/G snv 0.59 2