{{Rsnum
|rsid=2710057
|Chromosome=X
|position=86937000
|Orientation=plus
|GMAF=0.2304
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
}}{{ population diversity
| geno1=(G;G)
| geno2=(G;T)
| geno3=(T;T)
| CEU | 16.9 | 23.1 | 60.0
| HCB | 18.2 | 27.3 | 54.5
| JPT | 11.4 | 9.1 | 79.5
| YRI | 14.3 | 19.0 | 66.7
| ASW | 0.0 | 0.0 | 0.0
| CHB | 18.2 | 27.3 | 54.5
| CHD | 13.3 | 11.4 | 75.2
| GIH | 0.0 | 0.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 0.0 | 0.0 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 20.2 | 12.1 | 67.7
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19079262
|Trait=Bone mineral density (hip)
|Title=New sequence variants associated with bone mineral density
|RiskAllele=T
|Pval=0.000001
|OR=0.07
|ORtxt=[0.04-0.09] SD decrease
}}

{{PharmGKB
|RSID=rs2710057
|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: Xq21.2; Reported Gene(s): NR; Risk Allele: rs2710057-T); (p-value= 0.000001).This variant is associated with Bone mineral density (hip).
|Drugs=
|Drug Classes=
|Diseases=Bone Diseases; Bone Diseases, Metabolic
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA164740133
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs2710057
|overall_frequency_n=67
|overall_frequency_d=92
|overall_frequency=0.728261
|n_genomes=42
|n_genomes_annotated=0
|n_haplomes=76
|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}}