{{Rsnum
|rsid=7029536
|Gene=GARNL3
|Chromosome=9
|position=127348132
|Orientation=plus
|GMAF=0.343
|Gene_s=GARNL3
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 52.2 | 43.4 | 4.4
| HCB | 35.0 | 51.1 | 13.9
| JPT | 52.2 | 38.9 | 8.8
| YRI | 49.0 | 36.7 | 14.3
| ASW | 40.4 | 49.1 | 10.5
| CHB | 35.0 | 51.1 | 13.9
| CHD | 45.0 | 36.7 | 18.3
| GIH | 51.5 | 35.6 | 12.9
| LWK | 26.4 | 51.8 | 21.8
| MEX | 29.3 | 51.7 | 19.0
| MKK | 55.1 | 39.7 | 5.1
| TSI | 60.8 | 33.3 | 5.9
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23319000
  |Trait=Metabolite levels (HVA)
  |Title=Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.
  |RiskAllele=T
  |Pval=5E-6
  |OR=.23
  |ORtxt=unit decrease
  }}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | FTDNA2}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}