Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs4072037
MUC1
0.732 0.240 1 155192276 splice acceptor variant C/A;T snv 0.59 22
rs10754558
NLRP3
0.695 0.480 1 247448734 3 prime UTR variant G/C;T snv 20
rs17145750
MLXIPL
0.925 0.120 7 73612048 intron variant C/A;T snv 9
rs9472135
LOC107986598
0.925 0.120 6 43842065 intron variant T/A;C;G snv 9
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 8
rs11755724
RREB1
0.807 0.320 6 7118757 intron variant A/G;T snv 7
rs13022873
ZNF512
0.882 0.120 2 27592643 intron variant A/C;T snv 7
rs1394125
UBE2Q2
0.882 0.200 15 75866642 intron variant G/A;T snv 7
rs1572982
HFE
0.827 0.200 6 26094139 intron variant G/A;T snv 0.52; 8.0E-06 7
rs683369
SLC22A1
0.807 0.360 6 160130172 missense variant G/A;C;T snv 4.0E-06; 0.83; 4.0E-06 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
rs7691759 0.882 0.120 4 9686390 intron variant T/A;C snv 7
rs881858
LOC105375069 ; LOC107986598
0.882 0.200 6 43838872 intron variant G/A;C snv 7
rs2622621
ABCG2
0.851 0.240 4 88109768 intron variant C/A;G snv 6
rs4665987 0.925 0.120 2 27532958 upstream gene variant G/A;T snv 6
rs4666002
ZNF512
0.925 0.120 2 27617773 intron variant G/A;C 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
rs7753826 0.925 0.120 6 26042011 upstream gene variant T/A;C snv 6
rs115810
TRIM38
0.925 0.120 6 25975655 intron variant G/A;C snv 5
rs11983997 0.925 0.120 7 73524914 upstream gene variant G/A;C snv 5