{{Rsnum
|rsid=6442522
|Chromosome=3
|position=15399049
|Orientation=plus
|GMAF=0.478
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=METTL6
|Gene_s=METTL6
}}{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 30.1 | 47.8 | 22.1
| HCB | 28.5 | 47.4 | 24.1
| JPT | 21.2 | 48.7 | 30.1
| YRI | 6.1 | 44.9 | 49.0
| ASW | 12.3 | 43.9 | 43.9
| CHB | 28.5 | 47.4 | 24.1
| CHD | 13.8 | 45.0 | 41.3
| GIH | 25.7 | 55.4 | 18.8
| LWK | 12.7 | 44.5 | 42.7
| MEX | 27.6 | 50.0 | 22.4
| MKK | 12.2 | 46.8 | 41.0
| TSI | 22.5 | 59.8 | 17.6
| HapMapRevision=28
}}

{{GWAS Summary
|SNP=rs6442522
|PubMedID=18759275
|Condition=Serum uric acid
|Gene=NR
|Risk Allele=
|pValue=5.00E-006
|OR=0.05
|95CI=NR) mg/dl increase in uric acid level
|OA=1
}}

{{PharmGKB
|RSID=rs6442522
|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=PA162356401
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs6442522
|overall_frequency_n=64
|overall_frequency_d=118
|overall_frequency=0.542373
|n_genomes=39
|n_genomes_annotated=0
|n_haplomes=55
|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}}