Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs6554759 1.000 0.040 5 1316987 downstream gene variant G/A snv 0.85 1
rs2158041
AHR
0.807 0.160 7 17328796 intron variant T/C snv 0.81 6
rs828704
XRCC5
1.000 0.040 2 216128888 intron variant C/A snv 0.81 1
rs6062302
RTEL1 ; RTEL1-TNFRSF6B
0.882 0.040 20 63689615 synonymous variant T/C snv 0.74 0.81 1
rs2297440
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.080 20 63680946 intron variant T/C snv 0.81 9
rs10464870
CCDC26
0.882 0.040 8 129465577 intron variant C/T snv 0.80 2
rs1582417
MIR3142HG
0.925 0.040 5 160470494 intron variant A/G snv 0.80 2
rs2427824
FCER1A
1.000 0.040 1 159295272 intron variant T/C snv 0.79 1
rs3787016
POLR2E
0.677 0.280 19 1090804 intron variant A/G snv 0.78 24
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 47
rs324015
STAT6
0.827 0.120 12 57096317 3 prime UTR variant T/C snv 0.76 5
rs2157719
CDKN2B-AS1
0.708 0.360 9 22033367 non coding transcript exon variant C/T snv 0.71 14
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
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs2961920
MIR3142HG ; MIR146A
1.000 0.040 5 160484499 intron variant C/A snv 0.70 1
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 107
rs2278089
NMI
1.000 0.040 2 151290158 upstream gene variant G/T snv 0.69 1
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 81
rs7003908
PRKDC
0.716 0.320 8 47858141 intron variant C/A snv 0.66 15
rs4774756
RAB27A
1.000 0.040 15 55254859 intron variant A/C snv 0.66 1
rs2239647
AKAP6
0.851 0.080 14 32823537 synonymous variant A/C snv 0.60 0.65 3
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 16