{{Rsnum
|rsid=1990932
|Chromosome=19
|position=45937042
|Orientation=plus
|GMAF=0.4366
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=NOVA2
|Gene_s=NOVA2
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 17.7 | 47.8 | 34.5
| HCB | 10.2 | 40.1 | 49.6
| JPT | 16.8 | 46.9 | 36.3
| YRI | 31.3 | 49.7 | 19.0
| ASW | 28.1 | 52.6 | 19.3
| CHB | 10.2 | 40.1 | 49.6
| CHD | 13.8 | 45.9 | 40.4
| GIH | 16.8 | 47.5 | 35.6
| LWK | 20.9 | 53.6 | 25.5
| MEX | 39.7 | 51.7 | 8.6
| MKK | 30.8 | 56.4 | 12.8
| TSI | 17.8 | 61.4 | 20.8
| HapMapRevision=28
}}{{PMID Auto
|PMID=20133464
|Title=Identification of a Second Kindred with Familial Hypocalciuric Hypercalcemia Type 3 (FHH3) Narrows Localization to a &lt;3.5 Megabase Pair Region on Chromosome 19q13.3
}}

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