{{Rsnum
|rsid=6060369
|Gene=UQCC
|Chromosome=20
|position=35319358
|Orientation=plus
|GMAF=0.4298
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=UQCC1
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 12.4 | 42.5 | 45.1
| HCB | 5.8 | 39.4 | 54.7
| JPT | 9.7 | 31.9 | 58.4
| YRI | 63.3 | 29.9 | 6.8
| ASW | 43.9 | 43.9 | 12.3
| CHB | 5.8 | 39.4 | 54.7
| CHD | 9.2 | 33.9 | 56.9
| GIH | 45.5 | 43.6 | 10.9
| LWK | 71.8 | 25.5 | 2.7
| MEX | 10.3 | 25.9 | 63.8
| MKK | 55.8 | 36.5 | 7.7
| TSI | 21.6 | 51.0 | 27.5
| HapMapRevision=28
}}[[rs6060369]] is a SNP associated with a (slight) increase in height, in that individuals tend to be 0.44cm taller for each [[rs6060369]](C) allele they carry. This finding was statistically significant (p=9.7x10e-7), and ultimately tested in over 28,000 individuals.{{PMID|18193045|OA=1
}} 

A haplotype of [[rs6060369]] and [[rs143383]], a neighboring SNP in the [[GDF5]] gene, can be defined, which also links height to [[osteoarthritis]] since [[rs143383]] has previously been linked to [[osteoarthritis]].{{PMID|18193045|OA=1
}}

[http://www.medpagetoday.com/PublicHealthPolicy/Genetics/tb/7961 Medpage article]

{{GWAS Summary
|SNP=rs6060369
|PubMedID=18193045
|Condition=Height
|Gene=BFZB
|Risk Allele=C
|pValue=2.00E-016
|OR=0.44
|95CI=NR) cm talle
|OA=1
}}

{{PMID Auto GWAS
|PMID=18391950
|Trait=Height
|Title=Identification of ten loci associated with height highlights new biological pathways in human growth
|RiskAllele=C
|Pval=9.9999999999999998E-17
|OR=0.44
|ORtxt=[0.34-0.72] cm taller
|OA=1
}}

{{omim
|desc=STATURE QUANTITATIVE TRAIT LOCUS 14; STQTL14
|id=612228
|rsnum=6060369
}}

{{PharmGKB
|RSID=rs6060369
|Name_s=
|Gene_s=UQCC
|Feature=
|Evidence=PubMed ID:18193045; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS Results: Common variants in the GDF5-UQCC region are associated with variation in human height (Initial Sample Size: 6,669 individuals; Replication Sample Size: 28,801 individuals).
|Drugs=
|Drug Classes=
|Diseases=
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA162356726
}}

{{PMID|19030899|OA=1
}} Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.

{{PMID|19197348|OA=1
}} Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae.

{{PMID|20017971|OA=1
}} Assessing the impact of global versus local ancestry in association studies.

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6060369
|overall_frequency_n=65
|overall_frequency_d=126
|overall_frequency=0.515873
|n_genomes=37
|n_genomes_annotated=0
|n_haplomes=51
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}