{{Rsnum
|rsid=139909
|Gene=TNRC6B
|Chromosome=22
|position=40301577
|Orientation=plus
|GMAF=0.3186
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=TNRC6B
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 9.7 | 40.7 | 49.6
| HCB | 37.2 | 45.3 | 17.5
| JPT | 21.2 | 49.6 | 29.2
| YRI | 0.0 | 0.7 | 99.3
| ASW | 1.8 | 14.0 | 84.2
| CHB | 37.2 | 45.3 | 17.5
| CHD | 31.2 | 52.3 | 16.5
| GIH | 6.9 | 27.7 | 65.3
| LWK | 0.0 | 1.8 | 98.2
| MEX | 6.9 | 37.9 | 55.2
| MKK | 0.6 | 17.9 | 81.4
| TSI | 19.6 | 43.1 | 37.3
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19570815
|Trait=Height
|Title=A genome-wide association study of northwestern Europeans involves the CNP signaling pathway in the etiology of human height variation
|RiskAllele=T
|Pval=2E-7
|OR=0.25
|ORtxt=[0.03-0.47] cm increase
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs139909
|overall_frequency_n=95
|overall_frequency_d=126
|overall_frequency=0.753968
|n_genomes=48
|n_genomes_annotated=0
|n_haplomes=80
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v1}}
{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}