Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805097
IRS2
0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs773442580
EGF
0.851 0.080 4 109913367 missense variant T/C;G snv 4.0E-06 7
rs7993934
COL4A2
0.790 0.080 13 110422568 intron variant C/T snv 0.56 9
rs8000189
COL4A2
0.776 0.080 13 110423534 intron variant C/T snv 0.61 10
rs9481067
SLC22A16
0.776 0.080 6 110429349 intron variant A/G snv 0.58 10
rs10980628
LPAR1
0.776 0.080 9 110909123 intron variant T/C snv 0.16 10
rs4849303
ACOXL
0.790 0.080 2 110970905 intron variant C/G;T snv 9
rs3087967
C11orf53
0.776 0.080 11 111286111 3 prime UTR variant T/C snv 0.72 10
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 25
rs6589219
COLCA2 ; COLCA1
0.790 0.080 11 111302186 intron variant G/C snv 0.69 9
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs597808
ATXN2
0.742 0.200 12 111535554 intron variant A/G snv 0.67 19
rs12241008
VTI1A
0.716 0.160 10 112520943 intron variant T/C snv 0.13 16
rs12246635
VTI1A
0.776 0.080 10 112528860 intron variant T/C snv 0.13 10
rs12255141
VTI1A
0.790 0.080 10 112535133 intron variant A/G;T snv 9
rs10506868
VTI1A
0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 16
rs755229494
APC
0.776 0.080 5 112761654 intron variant A/G snv 9.6E-04 10
rs777980327
APC
0.716 0.280 5 112837567 missense variant A/T snv 4.0E-06 7.0E-06 21
rs1380087059
APC
0.882 0.160 5 112837749 missense variant G/C snv 4.0E-06 3
rs587781394
APC
0.882 0.160 5 112837812 missense variant G/A;C snv 4.0E-06; 8.0E-06 3
rs137854575
APC
0.807 0.120 5 112838399 stop gained C/A;G;T snv 4.7E-04 9
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 42
rs387906234
APC
0.827 0.120 5 112839979 frameshift variant AGAG/-;AG delins 7
rs459552
APC
0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 14