{{Rsnum
|rsid=314268
|Gene=LIN28B
|Chromosome=6
|position=104970103
|Orientation=minus
|GMAF=0.3696
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=LIN28B
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 7.1 | 58.0 | 34.8
| HCB | 8.2 | 36.6 | 55.2
| JPT | 1.8 | 49.1 | 49.1
| YRI | 17.1 | 51.4 | 31.5
| ASW | 19.3 | 54.4 | 26.3
| CHB | 8.2 | 36.6 | 55.2
| CHD | 7.4 | 47.2 | 45.4
| GIH | 11.9 | 46.5 | 41.6
| LWK | 21.3 | 62.0 | 16.7
| MEX | 1.8 | 46.4 | 51.8
| MKK | 25.0 | 49.4 | 25.6
| TSI | 8.8 | 45.1 | 46.1
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=18391951
|Trait=Height
|Title=Many sequence variants affecting diversity of adult human height
|RiskAllele=C
|Pval=7.9999999999999996E-7
|OR=4.60
|ORtxt=[2.84-6.36] % SD taller
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs314268
|overall_frequency_n=83
|overall_frequency_d=128
|overall_frequency=0.648438
|n_genomes=48
|n_genomes_annotated=0
|n_haplomes=72
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{on chip | 23andMe v2}}
{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Illumina Human 1M}}