Disease: Prostate specific antigen measurement
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4430796
HNF1B
0.790 0.280 17 37738049 intron variant A/G snv 0.52 5
rs7501939
HNF1B
0.776 0.280 17 37741165 intron variant C/T snv 0.41 4
rs10993994
MSMB
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54 3
rs2735839 0.827 0.160 19 50861367 upstream gene variant A/C;G snv 3
rs3744763
HNF1B
0.925 0.160 17 37730894 non coding transcript exon variant A/G snv 0.30 3
rs1058205
KLK3
0.925 0.080 19 50860142 3 prime UTR variant C/T snv 0.75 0.74 2
rs17632542
KLK3
0.925 0.080 19 50858501 missense variant T/C snv 5.5E-02 4.9E-02 2
rs266849
LOC105372441
0.925 0.080 19 50845834 intron variant G/A snv 0.82 2
rs266870
LOC105372441
1.000 0.080 19 50848678 intron variant T/C snv 0.43 2