Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2854509
XRCC1
0.807 0.160 19 43570445 intron variant T/G snv 0.80 6
rs3757441
EZH2
0.752 0.200 7 148827660 intron variant C/T snv 0.80 12
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 52
rs7689420
HHIP-AS1 ; HHIP
0.851 0.080 4 144647200 non coding transcript exon variant T/C snv 0.79 7
rs2895680
STK32A
0.882 0.080 5 147264552 intron variant C/T snv 0.79 3
rs36600
MTMR3
0.827 0.080 22 29941597 intron variant T/C snv 0.78 5
rs3206824
DKK3
0.827 0.160 11 11964514 missense variant T/C snv 0.78 0.78 6
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs2564978
CD55
0.827 0.080 1 207321071 upstream gene variant T/C snv 0.77 6
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs2808630 0.742 0.240 1 159711078 downstream gene variant C/T snv 0.77 13
rs3769201
MAP3K20
0.882 0.080 2 173091813 intron variant T/C snv 0.77 3
rs7811989
AHR
0.882 0.080 7 17331739 intron variant A/G snv 0.76 3
rs751402
ERCC5 ; BIVM-ERCC5
0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs1266828
IL17F
0.807 0.120 6 52243264 intron variant G/A snv 0.75 6
rs4246444
FASN
0.882 0.080 17 82081076 intron variant T/G snv 0.75 3
rs4957014
AHRR ; PDCD6
0.752 0.160 5 287899 intron variant T/G snv 0.74 11
rs1800797
IL6 ; IL6-AS1 ; STEAP1B
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs938682
CHRNA3
0.851 0.080 15 78604205 intron variant G/A snv 0.72 7
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
rs11637630
CHRNA3
0.882 0.080 15 78607377 intron variant G/A snv 0.71 6
rs459809
REV3L ; MFSD4B
0.882 0.080 6 111331964 intron variant T/C snv 0.71 3
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1878022
CMKLR1
0.851 0.080 12 108305255 intron variant C/T snv 0.70 4