{{Rsnum
|rsid=1776897
|Chromosome=6
|position=34227234
|Orientation=minus
|GMAF=0.2126
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;C)
| geno3=(C;C)
| CEU | 81.4 | 18.6 | 0.0
| HCB | 77.4 | 20.4 | 2.2
| JPT | 68.1 | 28.3 | 3.5
| YRI | 31.3 | 52.4 | 16.3
| ASW | 24.6 | 57.9 | 17.5
| CHB | 77.4 | 20.4 | 2.2
| CHD | 76.1 | 22.9 | 0.9
| GIH | 90.1 | 7.9 | 2.0
| LWK | 27.3 | 48.2 | 24.5
| MEX | 37.9 | 50.0 | 12.1
| MKK | 42.9 | 42.9 | 14.1
| TSI | 86.3 | 12.7 | 1.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19343178
|Trait=Height
|Title=Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size
|RiskAllele=
|Pval=8E-11
|OA=1
}}
{{PMID Auto GWAS
|PMID=18391951
|Trait=Height
|Title=Many sequence variants affecting diversity of adult human height
|RiskAllele=C
|Pval=1E-8
|OR=8.80
|ORtxt=[5.66-11.94] % SD taller
}}

{{PharmGKB
|RSID=rs1776897
|Name_s=
|Gene_s=HMGA1
|Feature=
|Evidence=PubMed ID:19343178; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: Meta-analysis of genome-wide scans for human adult stature identifies novel Loci and associations with measures of skeletal frame size. (Initial Sample Size: 12,611 individuals; Replication Sample Size: 7,187 individuals); (Region: 6p21.31; Reported Gene(s): HMGA1,C6orf106; Risk Allele: rs1776897-?); (p-value= 0.00000000008).This variant is associated with Height.
|Drugs=
|Drug Classes=
|Diseases=
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA164739868
}}

{{PMID Auto GWAS
|PMID=20397748
|Trait=Height
|Title=Genome-Wide Association Study of Height and Body Mass Index in Australian Twin Families
|RiskAllele=T
|Pval=0.000007
|OR=0.11
|ORtxt=[0.04-0.18] SD decrease
|OA=1
}}

{{omim
|id=612893
|rsnum=1776897
}}

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

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs1776897
|overall_frequency_n=61
|overall_frequency_d=74
|overall_frequency=0.824324
|n_genomes=30
|n_genomes_annotated=0
|n_haplomes=47
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

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