Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2071214
BIRC5
17 78223510 missense variant G/A snv 0.93 0.96 3
rs4759314
HOTAIR
0.649 0.440 12 53968051 non coding transcript exon variant G/A snv 0.93 31
rs11337
GOLGA7
0.925 0.120 8 41510767 3 prime UTR variant T/G snv 0.93 4
rs7581886
NPAS2
0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs406193 0.882 0.120 20 32811837 downstream gene variant T/C snv 0.91 5
rs4645878
BAX
0.882 0.120 19 48954681 upstream gene variant A/G snv 0.89 5
rs2705901
CASP3
4 184638333 intron variant G/C snv 0.88 2
rs629367
MIR100HG ; MIRLET7A2
0.776 0.200 11 122146306 intron variant C/A snv 0.88 11
rs9325782 0.851 0.120 8 16232964 intron variant C/T snv 0.87 6
rs2230229
TNFRSF10A
0.807 0.120 8 23191779 missense variant C/T snv 0.88 0.86 8
rs1887922
IDE
0.851 0.240 10 92464408 intron variant C/T snv 0.85 6
rs2494752
AKT1
0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10
rs1047972
AURKA
0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs7558615
ERBB4
0.925 0.080 2 212081424 intron variant T/C snv 0.84 4
rs7959129
ATF1
1.000 0.080 12 50775325 intron variant T/G snv 0.84 3
rs4819554
IL17RA
0.776 0.320 22 17084145 upstream gene variant G/A snv 0.84 10
rs132770
DESI1 ; XRCC6
0.752 0.320 22 41621260 5 prime UTR variant A/G snv 0.83 14
rs4544930
PTPRK ; LOC101928140
6 128073744 intron variant T/C snv 0.83 2
rs822396
ADIPOQ
0.732 0.400 3 186849088 intron variant G/A snv 0.81 16
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 24
rs2227564
PLAU ; C10orf55
0.763 0.320 10 73913343 missense variant T/C snv 0.75 0.81 15
rs2057482
HIF1A-AS2 ; HIF1A-AS3 ; HIF1A
0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs3757441
EZH2
0.752 0.200 7 148827660 intron variant C/T snv 0.80 12
rs1801132
ESR1
0.689 0.320 6 151944387 synonymous variant G/C snv 0.73 0.80 22
rs2740574
CYP3A4
0.807 0.360 7 99784473 upstream gene variant C/T snv 0.78 12