Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13241427 1.000 7 1249003 regulatory region variant G/T snv 0.72 6
rs12423664
FBRSL1
1.000 0.040 12 132493308 intron variant G/A snv 0.10 6
rs2244608
HNF1A ; HNF1A-AS1
0.882 0.160 12 120979185 intron variant A/G snv 0.29 6
rs3925584
LOC101928338
1.000 0.080 11 30738788 intergenic variant T/C snv 0.35 6
rs17050272
LOC105373585
0.882 0.120 2 120548864 upstream gene variant G/A snv 0.33 6
rs11099098 0.925 0.120 4 80248758 intergenic variant G/C;T snv 5
rs2472297 0.882 0.160 15 74735539 intergenic variant C/T snv 0.16 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
rs3782886
BRAP
0.724 0.480 12 111672685 synonymous variant T/C snv 1.9E-02 5.9E-03 5
rs62033406
FTO
16 53790314 intron variant A/G snv 0.33 5
rs3741414
INHBC
0.925 0.120 12 57450266 3 prime UTR variant C/T snv 0.19 5
rs79598313
KDF1
1 26958422 intron variant C/A;T snv 5
rs11072567
NRG4
15 76006403 intron variant A/G snv 0.43 5
rs186459505
SFMBT1
0.925 0.120 3 52907083 missense variant G/A;T snv 1.1E-04; 4.0E-06 5
rs1171614
SLC16A9
0.882 0.200 10 59709780 5 prime UTR variant T/C snv 0.79 5
rs149454410
SLC2A9
0.925 0.120 4 9942000 missense variant C/G;T snv 4.0E-05; 3.2E-04 5
rs17145738
TBL2
0.851 0.200 7 73568544 3 prime UTR variant C/T snv 0.11 5
rs10109414 1.000 0.080 8 23893638 regulatory region variant C/T snv 0.37 4
rs11663816 18 60208994 intergenic variant T/C snv 0.20 4
rs4014195 0.882 0.200 11 65739351 intergenic variant C/G snv 0.31 4
rs4766566
CUX2
0.851 0.200 12 111269073 intron variant C/T snv 0.42 4
rs626277
DACH1
1.000 0.080 13 71773564 intron variant A/C snv 0.51 4
rs9302635
DHX38
16 72110275 intron variant T/C;G snv 4