Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4919510
SEMA4G ; MIR608 ; MRPL43
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs2094258
ERCC5 ; BIVM-ERCC5
0.701 0.280 13 102844409 intron variant C/T snv 0.18 20
rs2296147
BIVM-ERCC5 ; ERCC5
0.695 0.280 13 102846025 5 prime UTR variant T/C snv 0.38 21
rs873601
BIVM-ERCC5 ; ERCC5
0.677 0.360 13 102875987 3 prime UTR variant G/A snv 0.59 25
rs2252070
MMP13
0.752 0.320 11 102955810 upstream gene variant C/T snv 0.68 13
rs8126
TNFAIP2
0.807 0.080 14 103137232 3 prime UTR variant C/T snv 0.63 8
rs1200003171
AKT1
0.882 0.120 14 104775122 missense variant C/A;T snv 8.0E-06 4
rs2494752
AKT1
0.790 0.120 14 104797271 upstream gene variant A/G snv 0.85 10
rs1322178
ATG5
1.000 0.080 6 106183905 intron variant C/T snv 0.15 1
rs3804329
ATG5
1.000 0.080 6 106238552 intron variant A/G snv 0.15 2
rs9034
NAMPT
0.827 0.200 7 106249610 3 prime UTR variant A/G;T snv 5
rs61330082
NAMPT
0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22 13
rs671116
ATG5
1.000 0.080 6 106312722 intron variant A/G snv 0.41 1
rs2294750 1.000 0.080 1 10824979 regulatory region variant G/A snv 0.10 1
rs664677
ATM
0.807 0.160 11 108272455 intron variant C/A;T snv 0.65 8
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs3219218
UNG
0.851 0.120 12 109100430 intron variant A/G snv 1.9E-02 4
rs246079
UNG
0.790 0.120 12 109109255 intron variant A/G;T snv 9
rs2237051
EGF
0.925 0.120 4 109980042 missense variant G/A snv 0.46 0.53 3
rs2536
MTOR
0.776 0.240 1 11106656 3 prime UTR variant T/C snv 5.8E-02 11
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs6573
RAP1A ; INKA2
1.000 0.080 1 111712767 3 prime UTR variant C/A snv 0.12 1
rs2399395
PLCXD2
1.000 0.080 3 111714647 intron variant T/C snv 0.96 1
rs197412
DDX20
1.000 0.080 1 111766331 missense variant T/C snv 0.43 0.49 2
rs886205
ALDH2
0.827 0.360 12 111766623 intron variant A/G snv 0.35 8