Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12241008
VTI1A
0.716 0.160 10 112520943 intron variant T/C snv 0.13 8
rs961253 0.732 0.240 20 6423634 intergenic variant C/A snv 0.34 7
rs150766139
NTHL1 ; TSC2
0.742 0.320 16 2046238 stop gained G/A snv 1.4E-03 1.4E-03 7
rs1321311 0.742 0.160 6 36655123 regulatory region variant C/A snv 0.28 6
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 6
rs4919687
CYP17A1
0.742 0.160 10 102835491 non coding transcript exon variant G/A snv 0.25 6
rs4925386
LAMA5
0.776 0.080 20 62345988 intron variant T/C snv 0.56 6
rs174537
TMEM258 ; MYRF
0.708 0.400 11 61785208 non coding transcript exon variant G/T snv 0.28 6
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 5
rs7014346
CASC8 ; POU5F1B ; PCAT1
0.732 0.240 8 127412547 intron variant A/G snv 0.63 5
rs2070699
EDN1
0.752 0.080 6 12292539 intron variant G/C;T snv 0.45 5
rs10411210
RHPN2
0.742 0.160 19 33041394 intron variant C/T snv 0.22 5
rs7229639
SMAD7
0.763 0.080 18 48924606 intron variant A/G snv 0.87 5
rs6691170 0.776 0.080 1 221872104 intergenic variant G/T snv 0.34 4
rs7931342 0.689 0.360 11 69227030 intergenic variant T/G snv 0.58 4
rs4143094
GATA3
0.752 0.240 10 8047173 intron variant T/G snv 0.70 4
rs11255841 0.776 0.080 10 8697617 intergenic variant T/A snv 0.25 3
rs12970291 0.763 0.120 18 75305279 intergenic variant G/A snv 2.8E-02 3
rs6687758 0.763 0.200 1 221991606 regulatory region variant A/G snv 0.20 3
rs11200014
FGFR2
0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 3
rs1665650
HSPA12A
0.752 0.160 10 116727589 intron variant T/C snv 0.69 3
rs11903757 0.763 0.160 2 191722478 intron variant T/C snv 0.16 2
rs16969681 0.776 0.080 15 32700910 downstream gene variant C/T snv 0.11 2
rs2965667 0.776 0.080 12 17291799 intergenic variant A/T snv 0.96 2
rs4813802 0.776 0.080 20 6718948 regulatory region variant T/G snv 0.28 2