{{Rsnum
|rsid=17690232
|Chromosome=4
|position=54368658
|Orientation=plus
|GMAF=0.09642
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;G)
| geno3=(G;G)
| CEU | 75.4 | 23.1 | 1.5
| HCB | 97.8 | 2.2 | 0.0
| JPT | 95.6 | 4.4 | 0.0
| YRI | 85.7 | 12.7 | 1.6
| ASW | 0.0 | 0.0 | 0.0
| CHB | 97.8 | 2.2 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 0.0 | 0.0 | 0.0
| HapMapRevision=28
}}{{GWAS Summary
|SNP=rs17690232
|PubMedID=18193045
|Condition=Height
|Gene=PDGFRA
|Risk Allele=C
|pValue=4.00E-007
|OR=0.86
|95CI=NR) cm talle
|OA=1
}}

{{PharmGKB
|RSID=rs17690232
|Name_s=
|Gene_s=-
|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=PA162356724
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs17690232
|overall_frequency_n=17
|overall_frequency_d=128
|overall_frequency=0.132812
|n_genomes=10
|n_genomes_annotated=0
|n_haplomes=10
|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 | HumanOmni1Quad}}