Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 23
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 17
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 16
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 10
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 7
rs2079742
BCAS3
0.851 0.240 17 61388336 non coding transcript exon variant T/C snv 0.20 7
rs9895661
BCAS3
0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69 7
rs2244608
HNF1A ; HNF1A-AS1
0.882 0.160 12 120979185 intron variant A/G snv 0.29 6
rs17050272
LOC105373585
0.882 0.120 2 120548864 upstream gene variant G/A snv 0.33 6
rs9472135
LOC107986598
0.925 0.120 6 43842065 intron variant T/A;C;G snv 6
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 5
rs7691759 0.882 0.120 4 9686390 intron variant T/A;C snv 5
rs1481012
ABCG2
0.882 0.200 4 88117930 intron variant A/G snv 8.9E-02 5
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 5
rs4148155
ABCG2
0.882 0.200 4 88133515 intron variant A/G snv 8.7E-02 5
rs7517847
IL23R ; C1orf141
0.689 0.600 1 67215986 intron variant T/G snv 0.37 5
rs3741414
INHBC
0.925 0.120 12 57450266 3 prime UTR variant C/T snv 0.19 5
rs11755724
RREB1
0.807 0.320 6 7118757 intron variant A/G;T snv 5
rs1171614
SLC16A9
0.882 0.200 10 59709780 5 prime UTR variant T/C snv 0.79 5
rs17145738
TBL2
0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11 5
rs4014195 0.882 0.200 11 65739351 intergenic variant C/G snv 0.31 4