Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2403254
HPS5
11 18303599 intron variant C/G;T snv 2
rs1495743 8 18415790 intergenic variant G/A;C snv 2
rs11705729
IGF2BP2
1.000 0.080 3 185789511 intron variant A/T snv 0.45 1
rs4253252
KLKB1
4 186236304 intron variant T/G snv 0.56 3
rs2023634
DGCR9 ; DGCR5
22 18984937 intron variant A/G snv 7.9E-02 2
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 6
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 7
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 3
rs9358356
CDKAL1
1.000 0.080 6 20667151 intron variant T/C snv 0.39 1
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 6
rs2216405 2 210752170 intergenic variant A/G snv 0.15 2
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 2
rs4149081
SLCO1B1
1.000 0.040 12 21225087 intron variant G/A snv 0.18 4
rs10799701 1 21494497 intergenic variant A/G snv 0.47 2
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 6
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 6
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 2
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs2624265
LINC02694
15 38856448 intron variant T/C snv 0.28 2
rs10518693
IVD
15 40407823 intron variant C/T snv 0.37 2
rs2971672
GCK
7 44166307 intron variant A/C snv 0.44 1
rs6975024
GCK
7 44192287 intron variant T/C snv 0.14 2
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 6