{{Rsnum
|rsid=7982677
|Gene=GPC5
|Chromosome=13
|position=92336070
|Orientation=plus
|GMAF=0.2971
|Gene_s=GPC5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 6.2 | 39.3 | 54.5
| HCB | 11.7 | 46.0 | 42.3
| JPT | 10.6 | 51.3 | 38.1
| YRI | 12.2 | 47.6 | 40.1
| ASW | 10.5 | 45.6 | 43.9
| CHB | 11.7 | 46.0 | 42.3
| CHD | 10.1 | 43.1 | 46.8
| GIH | 22.8 | 45.5 | 31.7
| LWK | 11.8 | 58.2 | 30.0
| MEX | 3.4 | 31.0 | 65.5
| MKK | 14.7 | 46.2 | 39.1
| TSI | 9.9 | 52.5 | 37.6
| HapMapRevision=28
}}Babies who are AC or AA at [[rs7982677]] are about 1.3-1.7 times more likely to have tetralogy of Fallot (TOF) http://blog.23andme.com/23andme-research/snpwatch/snpwatch-common-genetic-factors-associated-with-blue-babies/

{{PMID Auto GWAS
  |PMID=23297363
  |Trait=Tetralogy of Fallot
  |Title=Genome-wide association study identifies loci on 12q24 and 13q32 associated with Tetralogy of Fallot.
  |RiskAllele=A
  |Pval=3E-9
  |OR=1.29
  |ORtxt=[1.152-1.441]
  |OA=1
}}

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