Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12670403
LOC101927609 ; AHR
7 17269655 intron variant C/A snv 0.46 2
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 3
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 3
rs6558295
GPAA1
8 144084619 intron variant C/G snv 8.1E-02 0.14 2
rs662138
SLC22A1
6 160143444 intron variant C/G snv 0.14 2
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs2403254
HPS5
11 18303599 intron variant C/G;T snv 2
rs10096633 1.000 0.040 8 19973410 regulatory region variant C/T snv 0.22 7
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 6
rs4481233
SLC2A9
0.925 0.120 4 9954455 intron variant C/T snv 0.16 5
rs17168486
DGKB
1.000 0.080 7 14858657 intron variant C/T snv 0.18 3
rs10518693
IVD
15 40407823 intron variant C/T snv 0.37 2
rs612169
ABO
9 133268030 intron variant G/A snv 10
rs4149081
SLCO1B1
1.000 0.040 12 21225087 intron variant G/A snv 0.18 4
rs603424
PKD2L1
1.000 0.080 10 100315722 intron variant G/A snv 0.34 4
rs17277546
TRIM4
7 99891948 3 prime UTR variant G/A snv 3.1E-02 3
rs9393903
ELOVL2 ; ELOVL2-AS1
6 11042676 intron variant G/A snv 0.18 3
rs11185790
PANK1
10 89612776 intron variant G/A snv 0.15 2
rs12753193 1 65703996 non coding transcript exon variant G/A snv 0.58 2
rs1447352 11 92989595 downstream gene variant G/A snv 0.55 2
rs13391552
ALMS1
2 73591809 intron variant G/A;C snv 2
rs1495743 8 18415790 intergenic variant G/A;C snv 2
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 3
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12