{{Rsnum
|rsid=6085920
|Chromosome=20
|position=7199409
|Orientation=plus
|GMAF=0.2181
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=LOC101929265
|Gene_s=LOC101929265
}}{{ population diversity
| geno1=(A;A)
| geno2=(A;T)
| geno3=(T;T)
| CEU | 76.1 | 21.2 | 2.7
| HCB | 82.5 | 16.8 | 0.7
| JPT | 87.4 | 12.6 | 0.0
| YRI | 8.2 | 40.1 | 51.7
| ASW | 19.3 | 43.9 | 36.8
| CHB | 82.5 | 16.8 | 0.7
| CHD | 82.6 | 17.4 | 0.0
| GIH | 71.4 | 22.4 | 6.1
| LWK | 15.7 | 47.2 | 37.0
| MEX | 79.3 | 20.7 | 0.0
| MKK | 14.7 | 52.6 | 32.7
| TSI | 85.1 | 14.9 | 0.0
| HapMapRevision=28
}}

{{GWAS Summary
|SNP=rs6085920
|PubMedID=18759275
|Condition=Serum uric acid
|Gene=NR
|Risk Allele=
|pValue=6.00E-006
|OR=0.4
|95CI=NR) mg/dl decrease in uric acid level
|OA=1
}}

{{PharmGKB
|RSID=rs6085920
|Name_s=
|Gene_s=-
|Feature=
|Evidence=PubMed ID:18759275; Web Resource:http://www.genome.gov/gwastudies/
|Annotation=GWAS results: Association of a common nonsynonymous variant in GLUT9 with serum uric acid levels in old order amish (Initial Sample Size: 408 women, 460 men; Replication Sample Size: NR). This variant is associated with Serum uric acid levels.
|Drugs=
|Drug Classes=
|Diseases=
|Curation Level=Non-Curated
|PharmGKB Accession ID=PA162356403
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6085920
|overall_frequency_n=92
|overall_frequency_d=128
|overall_frequency=0.71875
|n_genomes=46
|n_genomes_annotated=0
|n_haplomes=78
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|in_pharmgkb=Y
|autoscore=2
|webscore=N
}}

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}
{{on chip | Affy GenomeWide 6}}
{{on chip | HumanOmni1Quad}}