Disease: Uric acid measurement (procedure)
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 12
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 8
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 7
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
rs12801636
PCNX3
1.000 0.040 11 65623846 intron variant G/A snv 0.25 4