Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs254942
ERCC4
0.882 0.080 16 13932150 splice region variant G/A;C;T snv 0.97; 4.0E-06; 4.0E-06 3
rs1229984
ADH1B
0.570 0.560 4 99318162 missense variant T/C;G snv 0.90 83
rs1679709
NKAPL ; ZKSCAN4
0.925 0.080 6 28260564 missense variant A/G snv 0.87 0.83 2
rs11084490
AURKC
0.925 0.080 19 57231104 5 prime UTR variant G/A;C;T snv 0.87; 3.8E-05 2
rs1047972
AURKA
0.716 0.240 20 56386407 missense variant T/C snv 0.85 0.84 19
rs2447867
ITGA1
0.925 0.080 5 52861540 missense variant T/C;G snv 0.79; 4.0E-06 2
rs4245739
MDM4
0.708 0.360 1 204549714 3 prime UTR variant C/A;G snv 0.77; 6.2E-06 21
rs2076167
PPARD
0.925 0.080 6 35424010 missense variant C/G;T snv 0.75 2
rs1064261
MTOR
0.925 0.080 1 11228701 missense variant G/A;T snv 0.75; 4.0E-06 3
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs10719
DROSHA
0.677 0.680 5 31401340 3 prime UTR variant A/G;T snv 0.69 24
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs2231231
AQP3
0.851 0.240 9 33442988 non coding transcript exon variant A/C snv 0.67 0.69 5
rs4626
TOB1
0.925 0.080 17 50863061 synonymous variant T/C snv 0.66 0.69 2
rs2241909
AURKB
0.925 0.080 17 8205021 synonymous variant G/A snv 0.66 0.64 2
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99
rs7813
GEMIN4
0.689 0.360 17 744946 missense variant G/A;C snv 0.63 22
rs1877031
STARD3
0.827 0.280 17 39657827 missense variant G/A snv 0.62 0.52 6
rs1058808
ERBB2
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs326222
DDB2
0.882 0.080 11 47238117 intron variant T/C snv 0.60 0.58 3
rs2292832
MIR149 ; GPC1 ; LOC100130449
0.605 0.640 2 240456086 non coding transcript exon variant T/A;C snv 0.59 46
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 22
rs238406
ERCC2
0.677 0.480 19 45365051 synonymous variant T/G snv 0.58 0.65 23