{{Rsnum
|rsid=11205277
|Gene=LOC100507640
|Chromosome=1
|position=149920979
|Orientation=plus
|GMAF=0.2897
|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 | 29.2 | 55.8 | 15.0
| HCB | 40.9 | 46.0 | 13.1
| JPT | 60.2 | 37.2 | 2.7
| YRI | 93.9 | 6.1 | 0.0
| ASW | 84.2 | 15.8 | 0.0
| CHB | 40.9 | 46.0 | 13.1
| CHD | 43.1 | 43.1 | 13.8
| GIH | 48.5 | 31.7 | 19.8
| LWK | 86.4 | 12.7 | 0.9
| MEX | 53.4 | 37.9 | 8.6
| MKK | 77.6 | 20.5 | 1.9
| TSI | 27.5 | 53.9 | 18.6
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=18391951
|Trait=Height
|Title=Many sequence variants affecting diversity of adult human height
|RiskAllele=G
|Pval=1E-10
|OR=5.10
|ORtxt=[3.53-6.67] % SD taller
}}

{{PMID Auto
|PMID=19039035
|Title=Genome-wide association study identifies two novel loci containing FLNB and SBF2 genes underlying stature variation.
|OA=1
}}

{{PMID Auto
|PMID=20546612
|Title=The role of height-associated loci identified in genome wide association studies in the determination of pediatric stature.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs11205277
|overall_frequency_n=31
|overall_frequency_d=128
|overall_frequency=0.242188
|n_genomes=18
|n_genomes_annotated=0
|n_haplomes=21
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{PMID Auto GWAS
  |PMID=20881960
  |Trait=Height
  |Title=Hundreds of variants clustered in genomic loci and biological pathways affect human height.
  |RiskAllele=A
  |Pval=5E-32
  |OR=.05
  |ORtxt=[NR] unit decrease
  |OA=1
}}

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