Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1394125
UBE2Q2
0.882 0.200 15 75866642 intron variant G/A;T snv 7
rs13241427 1.000 7 1249003 regulatory region variant G/T snv 0.72 6
rs1481012
ABCG2
0.882 0.200 4 88117930 intron variant A/G snv 8.9E-02 6
rs2622621
ABCG2
0.851 0.240 4 88109768 intron variant C/A;G snv 6
rs4766566
CUX2
0.851 0.200 12 111269073 intron variant C/T snv 0.42 6
rs12423664
FBRSL1
1.000 0.040 12 132493308 intron variant G/A snv 0.10 6
rs7756117
H3C3
0.882 0.160 6 26046337 upstream gene variant G/A snv 0.69 6
rs2032447
H3C3 ; H2BC3 ; H2AC5P
0.925 0.120 6 26044141 non coding transcript exon variant A/G snv 4.1E-06; 0.67 0.67 6
rs1800574
HNF1A ; HNF1A-AS1
0.882 0.080 12 120979061 missense variant C/T snv 2.9E-02 2.2E-02 6
rs729761
LOC105375069 ; LOC107986598
0.925 0.120 6 43836834 intron variant T/A;G snv 6
rs4886755
NRG4
0.925 0.120 15 76005791 non coding transcript exon variant A/G;T snv 0.49 6
rs10480300
PRKAG2
0.925 0.120 7 151708919 intron variant C/T snv 0.24 6
rs1171616
SLC16A9
0.882 0.200 10 59708831 intron variant G/T snv 0.79 6
rs11722228
SLC2A9
0.851 0.160 4 9914117 intron variant C/T snv 0.32 6
rs1014290
SLC2A9 ; LOC105374476
0.827 0.280 4 10000237 intron variant G/A snv 0.72 6
rs10109414 1.000 0.080 8 23893638 regulatory region variant C/T snv 0.37 5
rs1150660 0.925 0.120 6 26101212 upstream gene variant A/C snv 0.73 5
rs1967017 0.882 0.160 1 145711421 upstream gene variant A/G snv 0.43 5
rs199726 0.925 0.120 6 25953132 intergenic variant G/A snv 0.73 5
rs199734 0.925 0.120 6 25940165 intergenic variant G/A;C snv 5
rs199736 0.925 0.120 6 25936559 intergenic variant C/T snv 0.72 5
rs199737 0.925 0.120 6 25933310 upstream gene variant A/C;T snv 5
rs199739 0.925 0.120 6 25960281 upstream gene variant A/C;G snv 0.78 5
rs199750 0.882 0.160 6 26016234 upstream gene variant C/T snv 0.77 5
rs199751 0.925 0.120 6 26015355 upstream gene variant T/C snv 0.77 5