{{Rsnum
|rsid=16946160
|Gene=GPC5
|Chromosome=13
|position=91551559
|Orientation=plus
|GMAF=0.1607
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=GPC5
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 0.9 | 10.6 | 88.5
| HCB | 5.1 | 36.5 | 58.4
| JPT | 3.5 | 36.3 | 60.2
| YRI | 2.7 | 34.7 | 62.6
| ASW | 1.8 | 36.8 | 61.4
| CHB | 5.1 | 36.5 | 58.4
| CHD | 3.7 | 26.9 | 69.4
| GIH | 1.0 | 14.9 | 84.2
| LWK | 2.8 | 33.0 | 64.2
| MEX | 5.2 | 41.4 | 53.4
| MKK | 7.7 | 35.3 | 57.1
| TSI | 0.0 | 7.8 | 92.2
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21441931
|Trait=None
|Title=Common variation in GPC5 is associated with acquired nephrotic syndrome
|RiskAllele=A
|Pval=3E-7
|OR=1.3900
|ORtxt=[1.22-1.57]
}}

[[Kidney Disease]]

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}