{{Rsnum
|rsid=1371867
|Chromosome=8
|position=100317981
|Orientation=plus
|GMAF=0.4936
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=RNF19A
|Gene_s=RNF19A
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 29.2 | 51.3 | 19.5
| HCB | 28.5 | 51.1 | 20.4
| JPT | 27.4 | 46.0 | 26.5
| YRI | 4.8 | 29.3 | 66.0
| ASW | 8.8 | 36.8 | 54.4
| CHB | 28.5 | 51.1 | 20.4
| CHD | 27.5 | 44.0 | 28.4
| GIH | 20.8 | 50.5 | 28.7
| LWK | 6.4 | 39.1 | 54.5
| MEX | 39.7 | 44.8 | 15.5
| MKK | 9.6 | 40.4 | 50.0
| TSI | 40.2 | 46.1 | 13.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=21041692
|Trait=None
|Title=Identification of Genomic Predictors of Atrioventricular Conduction. Using Electronic Medical Records as a Tool for Genome Science
|RiskAllele=C
|Pval=0.000009
|OR=2.3200
|ORtxt=[1.30-3.34] ms increase
|OA=1
}}

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