Disease: Uric acid measurement (procedure)
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs334
HBB
0.724 0.240 11 5227002 missense variant T/A;C;G snv 3.5E-03 19
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 17
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs62435145 1.000 0.040 7 1246931 regulatory region variant G/T snv 0.51 8
rs760077
MTX1 ; THBS3
0.925 0.120 1 155208991 missense variant T/A snv 0.36 7
rs9895661
BCAS3
0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69 7
rs11072567
NRG4
15 76006403 intron variant A/G snv 0.43 5
rs13129697
SLC2A9
0.925 0.120 4 9925343 intron variant T/G snv 0.39 4
rs12987661
AAK1
2 69586326 intron variant T/C snv 0.11 2
rs7224610
HLF
0.925 0.120 17 55287427 intron variant C/A;G snv 2
rs744103
LOC105375069 ; LOC107986598
0.925 0.120 6 43837625 intron variant T/A snv 0.58 2