{{Rsnum
|rsid=4670779
|Gene=LOC344382
|Chromosome=2
|position=37817201
|Orientation=plus
|ReferenceAllele=C
|MissenseAllele=T
|GMAF=0.2167
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 48.2 | 44.6 | 7.1
| HCB | 52.2 | 36.6 | 11.2
| JPT | 47.8 | 43.4 | 8.8
| YRI | 96.5 | 3.5 | 0.0
| ASW | 91.2 | 8.8 | 0.0
| CHB | 52.2 | 36.6 | 11.2
| CHD | 50.5 | 41.0 | 8.6
| GIH | 52.0 | 44.0 | 4.0
| LWK | 93.5 | 5.6 | 0.9
| MEX | 46.6 | 46.6 | 6.9
| MKK | 91.0 | 8.4 | 0.6
| TSI | 47.0 | 45.0 | 8.0
| HapMapRevision=28
}}
{{PMID Auto GWAS
|PMID=19079262
|Trait=Bone mineral density (spine)
|Title=New sequence variants associated with bone mineral density
|RiskAllele=T
|Pval=0.000004
|OR=0.07
|ORtxt=[0.04-0.10] SD decrease
}}

{{PharmGKB
|RSID=rs4670779
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:19079262; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: New sequence variants associated with bone mineral density. (Initial Sample Size: 6,865 individuals; Replication Sample Size: 8,510 individuals); (Region: 2p22.2; Reported Gene(s): LOC344382; Risk Allele: rs4670779-T); (p-value= 0.000004).This variant is associated with Bone mineral density (spine).
|Drugs=
|Drug Classes=
|Diseases=Bone Diseases; Bone Diseases, Metabolic
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA164740141
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs4670779
|overall_frequency_n=23
|overall_frequency_d=128
|overall_frequency=0.179688
|n_genomes=14
|n_genomes_annotated=0
|n_haplomes=15
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

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