Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs577259500 0.925 0.120 4 10136132 intergenic variant -/C;CC ins 3
rs201759493 0.925 0.120 4 10207628 intergenic variant GG/- del 2.5E-02 3
rs35385468 0.925 0.120 6 26101212 upstream gene variant -/C delins 9.7E-03 5
rs386406569 0.925 0.120 6 26101212 upstream gene variant -/C delins 5
rs199984580 0.925 0.120 4 10179020 intergenic variant G/- delins 3
rs200251830
WDR1
0.925 0.120 4 10073861 upstream gene variant -/AT delins 3
rs371398607 0.925 0.120 4 10386987 intergenic variant T/- delins 3
rs386671621 0.925 0.120 4 10207628 intergenic variant GGTAGTTAT/TATATA delins 3
rs576402731 0.925 0.120 4 10179020 intergenic variant G/- delins 3
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 45
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 35
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 30
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 27
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 24
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 22
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
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 21