Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3817466
EPB41L3
18 5410575 synonymous variant A/G snv 0.86 0.75 1
rs2305160
NPAS2 ; NPAS2-AS1
0.776 0.200 2 100974842 missense variant A/G snv 0.71 0.75 9
rs9306160
RRP1B
0.925 0.080 21 43687681 missense variant T/C snv 0.69 0.73 3
rs1800797
IL6 ; IL6-AS1 ; STEAP1B
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs8176329
TIMP2
17 78856015 3 prime UTR variant G/A snv 0.71 1
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
rs2269700
DELEC1
9 115401284 non coding transcript exon variant C/T snv 0.67 0.71 1
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
rs461404
PRKAA1
0.925 0.080 5 40799438 upstream gene variant G/A snv 0.70 3
rs4646
MIR4713HG ; CYP19A1
0.716 0.360 15 51210647 3 prime UTR variant A/C snv 0.67 0.70 16
rs4562
ELP5 ; CLDN7
0.925 0.080 17 7260420 missense variant A/G snv 0.65 0.70 3
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 70
rs154268
PRKAA1
0.925 0.080 5 40795766 intron variant C/T snv 0.69 3
rs1805105
AXIN1
0.776 0.280 16 346264 synonymous variant A/G snv 0.61 0.69 11
rs7187167 1.000 0.040 16 1299208 upstream gene variant T/C snv 0.69 2
rs889312 0.732 0.360 5 56736057 regulatory region variant C/A snv 0.69 13
rs2010963
VEGFA
0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 81
rs308379
FGF2
1.000 0.080 4 122861741 intron variant A/T snv 0.68 2
rs11895168
ERBB4
0.925 0.080 2 211377467 3 prime UTR variant A/C snv 0.68 4
rs4796793
STAT3
0.716 0.320 17 42390192 upstream gene variant G/C snv 0.67 16
rs762551
CYP1A2
0.701 0.400 15 74749576 intron variant C/A snv 0.67 23
rs1823023
PIK3R1
5 68250578 intron variant A/G snv 0.66 1
rs4796030
LIG3
0.827 0.120 17 35003131 3 prime UTR variant A/C snv 0.66 6