Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 70
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 19
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 17
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 16
rs12953717
SMAD7
0.724 0.240 18 48927559 intron variant C/T snv 0.36 11
rs11196172
TCF7L2
0.708 0.200 10 112967084 intron variant G/A snv 0.13 10
rs10506868
VTI1A
0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 8
rs12241008
VTI1A
0.716 0.160 10 112520943 intron variant T/C snv 0.13 8
rs7758229
SLC22A3
0.732 0.120 6 160419220 intron variant G/A;T snv 8
rs9929218
CDH1
0.732 0.160 16 68787043 intron variant G/A snv 0.28 8
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 6
rs4925386
LAMA5
0.776 0.080 20 62345988 intron variant T/C snv 0.56 6
rs10411210
RHPN2
0.742 0.160 19 33041394 intron variant C/T snv 0.22 5
rs2070699
EDN1
0.752 0.080 6 12292539 intron variant G/C;T snv 0.45 5
rs7014346
CASC8 ; POU5F1B ; PCAT1
0.732 0.240 8 127412547 intron variant A/G snv 0.63 5
rs7229639
SMAD7
0.763 0.080 18 48924606 intron variant A/G snv 0.87 5
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 5
rs4143094
GATA3
0.752 0.240 10 8047173 intron variant T/G snv 0.70 4
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
rs11874392
SMAD7
0.763 0.080 18 48926786 intron variant A/T snv 0.50 2
rs11903757 0.763 0.160 2 191722478 intron variant T/C snv 0.16 2
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 2
rs2238126
ETV6
0.776 0.080 12 11856807 intron variant A/G snv 0.18 2
rs56848936
SYMPK
0.776 0.080 19 45818249 intron variant A/G snv 1.9E-02 2