Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 35
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 22
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs198851
H4C3
6 26104404 downstream gene variant T/A;C;G snv 15
rs174594
FADS2
0.776 0.160 11 61852357 intron variant C/A;T snv 14
rs17145750
MLXIPL
0.925 0.120 7 73612048 intron variant C/A;T snv 9
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 8
rs121907892
SLC22A12
0.807 0.240 11 64593747 stop gained G/A;C snv 2.8E-04 8
rs1394125
UBE2Q2
0.882 0.200 15 75866642 intron variant G/A;T snv 7
rs734553
SLC2A9
0.851 0.240 4 9921380 intron variant G/A;T snv 7
rs737267
SLC2A9
0.851 0.240 4 9933120 intron variant G/A;T snv 7
rs2622621
ABCG2
0.851 0.240 4 88109768 intron variant C/A;G snv 6
rs4886755
NRG4
0.925 0.120 15 76005791 non coding transcript exon variant A/G;T snv 0.49 6
rs729761
LOC105375069 ; LOC107986598
0.925 0.120 6 43836834 intron variant T/A;G snv 6
rs115810
TRIM38
0.925 0.120 6 25975655 intron variant G/A;C snv 5
rs12908437
IGF1R
0.882 0.200 15 98744146 intron variant T/C;G snv 5
rs149454410
SLC2A9
0.925 0.120 4 9942000 missense variant C/G;T snv 4.0E-05; 3.2E-04 5
rs1540276
H4C2
0.925 0.120 6 26028591 upstream gene variant T/A;G snv 5
rs174455
FADS3
1.000 0.080 11 61888645 intron variant G/A;C snv 5
rs1800977
ABCA1 ; LOC105376196
0.851 0.240 9 104928169 intron variant G/A;C snv 5
rs186459505
SFMBT1
0.925 0.120 3 52907083 missense variant G/A;T snv 1.1E-04; 4.0E-06 5
rs199734 0.925 0.120 6 25940165 intergenic variant G/A;C snv 5
rs199737 0.925 0.120 6 25933310 upstream gene variant A/C;T snv 5