{{Rsnum
|rsid=1812175
|Gene=HHIP
|Chromosome=4
|position=144653692
|Orientation=minus
|GMAF=0.2585
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene_s=HHIP
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 68.8 | 29.5 | 1.8
| HCB | 33.3 | 50.4 | 16.3
| JPT | 31.2 | 56.2 | 12.5
| YRI | 49.7 | 40.1 | 10.2
| ASW | 63.2 | 31.6 | 5.3
| CHB | 33.3 | 50.4 | 16.3
| CHD | 27.1 | 57.9 | 15.0
| GIH | 75.8 | 20.2 | 4.0
| LWK | 64.2 | 31.2 | 4.6
| MEX | 63.2 | 31.6 | 5.3
| MKK | 38.7 | 45.2 | 16.1
| TSI | 69.6 | 27.5 | 2.9
| HapMapRevision=28
}}

{{GWAS Summary
|SNP=rs1812175
|PubMedID=18391951
|Condition=Height
|Gene=HHIP
|Risk Allele=C
|pValue=1.00E-011
|OR=8.3
|95CI=5.95-10.65) % SD talle
}}

{{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=0.000004
|OA=1
}}

{{omim
|desc=STATURE QUANTITATIVE TRAIT LOCUS 12; STQTL12
|id=612224
|rsnum=1812175
}}

{{PharmGKB
|RSID=rs1812175
|Name_s=
|Gene_s=HHIP
|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: 4q31.22; Reported Gene(s): HHIP); (p-value= 0.000004).This variant is associated with Height.
|Drugs=
|Drug Classes=
|Diseases=
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA164739873
}}

{{PMID Auto GWAS
|PMID=20397748
|Trait=Height
|Title=Genome-Wide Association Study of Height and Body Mass Index in Australian Twin Families
|RiskAllele=C
|Pval=1E-9
|OR=0.12
|ORtxt=[0.07-0.17] SD decrease
|OA=1
}}

{{PharmGKB
|RSID=rs1812175
|Name_s=
|Gene_s=HHIP
|Feature=
|Evidence=PubMed ID:18391951; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS Results: Many sequence variants affecting diversity of adult human height (Initial Sample Size: 30,968 individuals; Replication Sample Size: 8,541 individuals).
|Drugs=
|Drug Classes=
|Diseases=
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA162356782
}}

{{PMID Auto
|PMID=19030899
|Title=Genome-wide association scan for stature in Chinese: evidence for ethnic specific loci.
|OA=1
}}

{{PMID Auto
|PMID=19197348
|Title=Genome-wide association studies in an isolated founder population from the Pacific Island of Kosrae.
|OA=1
}}

{{PMID Auto
|PMID=20017971
|Title=Assessing the impact of global versus local ancestry in association studies.
|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=rs1812175
|overall_frequency_n=104
|overall_frequency_d=128
|overall_frequency=0.8125
|n_genomes=51
|n_genomes_annotated=0
|n_haplomes=86
|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 | Affy GenomeWide 6}}
{{on chip | Illumina Human 1M}}