{{Rsnum
|rsid=9488238
|Gene=VN1R13P
|Chromosome=6
|position=113695931
|Orientation=plus
|GMAF=0.03765
|Gene_s=VN1R13P
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;G)
| geno3=(G;G)
| CEU | 95.6 | 4.4 | 0.0
| HCB | 98.5 | 1.5 | 0.0
| JPT | 89.4 | 10.6 | 0.0
| YRI | 77.6 | 17.0 | 5.4
| ASW | 80.7 | 19.3 | 0.0
| CHB | 98.5 | 1.5 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 93.1 | 6.9 | 0.0
| LWK | 79.1 | 20.9 | 0.0
| MEX | 96.6 | 3.4 | 0.0
| MKK | 91.7 | 7.7 | 0.6
| TSI | 93.1 | 6.9 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
  |PMID=22993228
  |Trait=Disc degeneration (lumbar)
  |Title=Novel genetic variants associated with lumbar disc degeneration in northern Europeans: a meta-analysis of 4600 subjects.
  |RiskAllele=A
  |Pval=5E-6
  |OR=.28
  |ORtxt=[0.16-0.40] unit decrease
  |OA=1
}}

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