Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs626277
DACH1
1.000 0.080 13 71773564 intron variant A/C snv 0.51 4
rs3114018
ABCG2
0.882 0.160 4 88143429 intron variant A/C snv 0.48 2
rs7212936
SERPINF2
17 1743357 intron variant A/C snv 0.46 2
rs11070231
FSIP1
15 39729375 intron variant A/C snv 0.44 1
rs12484795
PNPLA3
22 43947746 intron variant A/C snv 0.21 1
rs1649078
BICC1
10 58533560 intron variant A/C snv 0.45 1
rs188917216 4 87951768 regulatory region variant A/C snv 5.5E-03 1
rs346750
MARK4 ; EXOC3L2
19 45233960 intron variant A/C snv 0.41 1
rs56106601 9 128008205 intergenic variant A/C snv 9.4E-02 1
rs56230350
NFATC3
16 68133068 intron variant A/C snv 0.13 1
rs57440165
GUSBP2
6 26875738 intron variant A/C snv 5.6E-02 1
rs71456318
SLC22A11
11 64565390 non coding transcript exon variant A/C snv 0.39 0.37 1
rs74440730
CUBN
10 16878893 intron variant A/C snv 8.7E-02 1
rs9416703
BICC1
10 58523248 intron variant A/C snv 0.46 1
rs11949767
MXD3
1.000 0.080 5 177313243 upstream gene variant A/C;G snv 1
rs1574430
SLC22A7 ; CRIP3
6 43301291 intron variant A/C;G snv 0.55 1
rs56223908
SLC2A9
4 9916868 intron variant A/C;G snv 5.8E-02 1
rs57070985
KDM4B
19 4969042 upstream gene variant A/C;G snv 1
rs625172
PYGM
11 64754594 intron variant A/C;G snv 1
rs9394948
ZNF318
6 43367017 intron variant A/C;G snv 1
rs1165152
SLC17A1
0.925 0.120 6 25818538 intron variant A/C;G;T snv 1
rs7678287
SLC2A9 ; LOC105374476
1.000 0.080 4 9998877 intron variant A/C;G;T snv 1
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 8
rs12501884 4 9453964 downstream gene variant A/C;T snv 1
rs2645477
VMP1
17 59768263 intron variant A/C;T snv 1