{{Rsnum
|rsid=4802666
|Gene=MYH14
|Chromosome=19
|position=50217817
|Orientation=plus
|GMAF=0.2319
|Gene_s=MYH14
|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 | 6.2 | 44.2 | 49.6
| HCB | 8.1 | 46.3 | 45.6
| JPT | 6.2 | 42.5 | 51.3
| YRI | 0.0 | 13.2 | 86.8
| ASW | 3.5 | 19.3 | 77.2
| CHB | 8.1 | 46.3 | 45.6
| CHD | 4.6 | 39.4 | 56.0
| GIH | 8.1 | 49.5 | 42.4
| LWK | 0.0 | 23.6 | 76.4
| MEX | 5.3 | 29.8 | 64.9
| MKK | 1.9 | 29.5 | 68.6
| TSI | 2.9 | 44.1 | 52.9
| 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=.13
  |ORtxt=[0.073-0.187] unit decrease
  |OA=1
}}

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