{{Rsnum
|rsid=11031492
|Gene=WDHD1
|Chromosome=11
|position=31863373
|Orientation=plus
|GMAF=0.1162
|Gene_s=WDHD1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 0.0 | 9.1 | 90.9
| HCB | 0.0 | 2.4 | 97.6
| JPT | 0.0 | 2.6 | 97.4
| YRI | 0.0 | 0.0 | 100.0
| ASW | 0.0 | 0.0 | 0.0
| CHB | 0.0 | 2.4 | 97.6
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=23319000
  |Trait=Metabolite levels (HVA/5-HIAA ratio)
  |Title=Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.
  |RiskAllele=G
  |Pval=4E-6
  |OR=.22
  |ORtxt=unit increase
  }}

{{on chip | FTDNA}}