Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7094971
SLC16A9
0.925 0.120 10 59689806 intron variant A/G snv 0.13 4
rs4149081
SLCO1B1
1.000 0.040 12 21225087 intron variant G/A snv 0.18 4
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 4
rs10244051 1.000 0.080 7 15024208 intergenic variant T/A;G snv 3
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 3
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 3
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 3
rs17168486
DGKB
1.000 0.080 7 14858657 intron variant C/T snv 0.18 3
rs9393903
ELOVL2 ; ELOVL2-AS1
6 11042676 intron variant G/A snv 0.18 3
rs8396
ETFDH ; PPID
4 158709665 3 prime UTR variant T/C snv 0.29 3
rs4253252
KLKB1
4 186236304 intron variant T/G snv 0.56 3
rs7760535
REV3L ; MFSD4B
6 111425880 intron variant G/C snv 0.46 3
rs13266634
SLC30A8 ; LOC105375716
0.724 0.480 8 117172544 missense variant C/A;T snv 0.29 3
rs211718
SLC44A5
1 75640990 downstream gene variant T/C snv 0.75 3
rs17277546
TRIM4
7 99891948 3 prime UTR variant G/A snv 3.1E-02 3
rs2066938
UNC119B ; MIR4700
12 120722812 3 prime UTR variant A/C;G snv 3
rs10799701 1 21494497 intergenic variant A/G snv 0.47 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
rs1495743 8 18415790 intergenic variant G/A;C snv 2
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 2
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
rs494562 6 85407411 intergenic variant A/G snv 0.16 2
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 2