Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2965667 0.776 0.080 12 17291799 intergenic variant A/T snv 0.96 10
rs209489
ELOVL5
0.790 0.080 6 53312880 intron variant C/A snv 0.92 9
rs629849
IGF2R
0.827 0.160 6 160073377 missense variant A/C;G;T snv 0.90 0.91 9
rs7229639
SMAD7
0.763 0.080 18 48924606 intron variant A/G snv 0.87 13
rs2738783
RTEL1 ; RTEL1-TNFRSF6B
0.763 0.160 20 63677259 intron variant T/G snv 0.85 11
rs10849432
LOC105369625
0.790 0.080 12 6276561 intergenic variant C/T snv 0.84 9
rs1950902
MTHFD1
0.776 0.240 14 64415662 missense variant A/G snv 0.83 0.83 11
rs4378954
LSAMP
0.790 0.080 3 115931601 intron variant T/C snv 0.83 10
rs3775292
TLR3
0.851 0.080 4 186081871 non coding transcript exon variant C/G snv 0.82 5
rs1801132
ESR1
0.689 0.320 6 151944387 synonymous variant G/C snv 0.73 0.80 22
rs680
IGF2 ; INS-IGF2
0.925 0.080 11 2132404 3 prime UTR variant T/C;G snv 0.78 2
rs13831
GNAS
0.790 0.080 20 58900136 3 prime UTR variant A/G snv 0.77 9
rs9271770 0.776 0.120 6 32626471 upstream gene variant G/A snv 0.76 10
rs9271695 0.776 0.080 6 32625303 upstream gene variant A/G snv 0.76 10
rs6474387
IKBKB
0.882 0.080 8 42328734 intron variant T/C snv 0.76 3
rs1028166
TENM3 ; TENM3-AS1
0.790 0.080 4 181892145 intron variant G/A snv 0.74 9
rs6031311
TOX2
0.776 0.080 20 44037835 intron variant C/T snv 0.73 10
rs3087967
C11orf53
0.776 0.080 11 111286111 3 prime UTR variant T/C snv 0.72 10
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
rs2179593
TOX2
0.790 0.080 20 44031646 intron variant C/A snv 0.71 11
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 25
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193