Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7372209
CTDSPL ; MIR26A1
0.807 0.160 3 37969217 intron variant T/C snv 0.77 7
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 47
rs2808630 0.742 0.240 1 159711078 downstream gene variant C/T snv 0.77 13
rs751402
ERCC5 ; BIVM-ERCC5
0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs6474387
IKBKB
0.882 0.080 8 42328734 intron variant T/C snv 0.76 3
rs361863
ISX
1.000 0.080 22 35067169 missense variant A/G snv 0.71 0.73 1
rs1329149
CYP2E1
0.925 0.080 10 133536297 intron variant T/C snv 0.73 2
rs1549637
CABP5 ; PLA2G4C
0.925 0.120 19 48048700 intron variant A/T snv 0.72 3
rs10891246
COLCA1 ; COLCA2
1.000 0.080 11 111299815 missense variant A/G snv 0.72 1
rs3087967
C11orf53
0.776 0.080 11 111286111 3 prime UTR variant T/C snv 0.72 1
rs1444601
TOPBP1
1.000 0.080 3 133611099 synonymous variant G/A snv 0.69 0.72 1
rs10929732
ROCK2
1.000 0.080 2 11343366 intron variant A/G snv 0.72 2
rs2059691
CHROMR ; PRKRA
0.882 0.080 2 178437157 intron variant A/G snv 0.72 3
rs5743810
TLR6 ; TLR1
0.689 0.360 4 38828729 missense variant A/G snv 0.73 0.72 20
rs391957
HSPA5 ; LOC107987127
0.763 0.240 9 125241745 non coding transcript exon variant T/C snv 0.72 10
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 17
rs11987193 1.000 0.080 8 29478491 intergenic variant T/C snv 0.71 1
rs12071124
FH
1.000 0.080 1 241520405 upstream gene variant C/A;T snv 0.71 1
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs7130173
C11orf53
1.000 0.080 11 111283347 intron variant A/C snv 0.70 1
rs26279
MSH3
0.790 0.160 5 80873118 missense variant G/A snv 0.73 0.70 9
rs1391441
TET2-AS1 ; TET2
0.763 0.240 4 105207603 intron variant G/A snv 0.70 1
rs9588884 1.000 0.080 13 90145067 intergenic variant C/G snv 0.70 1