Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs629849
IGF2R
0.827 0.160 6 160073377 missense variant A/C;G;T snv 0.90 0.91 8
rs1950902
MTHFD1
0.776 0.240 14 64415662 missense variant A/G snv 0.83 0.83 10
rs3775292
TLR3
0.851 0.080 4 186081871 non coding transcript exon variant C/G snv 0.82 5
rs680
IGF2 ; INS-IGF2
0.925 0.080 11 2132404 3 prime UTR variant T/C;G snv 0.78 2
rs6474387
IKBKB
0.882 0.080 8 42328734 intron variant T/C snv 0.76 3
rs2059691
CHROMR ; PRKRA
0.882 0.080 2 178437157 intron variant A/G snv 0.72 3
rs1800797
IL6 ; IL6-AS1 ; STEAP1B
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs4147536
ADH1B
0.925 0.080 4 99317955 non coding transcript exon variant A/C snv 0.71 2
rs25487
XRCC1
0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 17
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs4562
ELP5 ; CLDN7
0.925 0.080 17 7260420 missense variant A/G snv 0.65 0.70 3
rs6588147
LEPR
0.851 0.080 1 65469811 intron variant G/A snv 0.70 4
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 70
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 81
rs2228226
GLI1 ; ARHGAP9
0.851 0.160 12 57472038 missense variant G/C snv 0.60 0.68 6
rs4779584 0.732 0.160 15 32702555 intergenic variant T/C snv 0.67 8
rs6598964
LIN28A
0.882 0.080 1 26419836 intron variant A/G snv 0.67 3
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 32
rs283415
ADH1C ; ADH1B
0.925 0.080 4 99349450 intron variant C/T snv 0.64 2
rs2470144
CYP19A1
0.925 0.080 15 51329528 intron variant T/C snv 0.60 2
rs9365723
SYNJ2
0.827 0.080 6 158014540 intron variant A/C;G snv 0.56 5
rs4678174
CASR
0.925 0.080 3 122282024 intron variant C/T snv 0.56 2
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs352139
TLR9
0.732 0.320 3 52224356 intron variant T/C snv 0.51 0.54 18