Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4113819 3 165758238 intron variant A/C;G snv 1
rs4675348 2 203577724 intergenic variant A/C;G snv 1
rs7581515 2 203228317 downstream gene variant A/C;G snv 1
rs7624915 3 165621222 intron variant A/C;G snv 1
rs7647059 3 166009894 intergenic variant A/C;G snv 1
rs7310409
HNF1A
0.925 0.160 12 120987058 intron variant A/C;G;T snv 3
rs4680662
BCHE
3 165798762 intron variant A/C;G;T snv 1
rs6715752
NBEAL1
2 203048829 intron variant A/C;G;T snv 1
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 6
rs4975709
IRX4
5 1877166 downstream gene variant A/C;T snv 1
rs6789103 3 166214169 intergenic variant A/C;T snv 1
rs9847379 3 165886202 regulatory region variant A/C;T snv 0.14 1
rs9883028 3 166079838 intergenic variant A/C;T snv 0.35 1
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 9
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 8
rs12678919 0.882 0.080 8 19986711 intergenic variant A/G snv 1.0E-01 7
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 7
rs2083637 0.925 0.080 8 20007664 intergenic variant A/G snv 0.25 6
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 6
rs11076175
CETP
16 56972466 intron variant A/G snv 0.20 5
rs6855911
SLC2A9
0.851 0.200 4 9934286 intron variant A/G snv 0.33 4
rs7442295
SLC2A9
0.925 0.120 4 9964756 intron variant A/G snv 0.28 4