{{Rsnum
|rsid=10046257
|Chromosome=6
|position=32886920
|Orientation=plus
|GMAF=0.1575
|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 | 0.9 | 15.9 | 83.2
| HCB | 1.5 | 27.7 | 70.8
| JPT | 2.7 | 21.2 | 76.1
| YRI | 4.8 | 36.1 | 59.2
| ASW | 0.0 | 38.6 | 61.4
| CHB | 1.5 | 27.7 | 70.8
| CHD | 4.6 | 21.1 | 74.3
| GIH | 4.0 | 16.8 | 79.2
| LWK | 3.6 | 43.6 | 52.7
| MEX | 5.2 | 32.8 | 62.1
| MKK | 1.9 | 30.8 | 67.3
| TSI | 4.9 | 25.5 | 69.6
| 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=3E-7
  |OR=.19
  |ORtxt=[0.12-0.26] unit increase
  |OA=1
}}

{{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}}