{{Rsnum
|rsid=154659
|Chromosome=16
|position=89600929
|Orientation=plus
|GMAF=0.36
|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 | 9.8 | 38.4 | 51.8
| HCB | 14.6 | 52.6 | 32.8
| JPT | 8.8 | 44.2 | 46.9
| YRI | 32.7 | 44.9 | 22.4
| ASW | 19.3 | 40.4 | 40.4
| CHB | 14.6 | 52.6 | 32.8
| CHD | 12.8 | 42.2 | 45.0
| GIH | 4.0 | 40.6 | 55.4
| LWK | 29.1 | 47.3 | 23.6
| MEX | 12.1 | 56.9 | 31.0
| MKK | 12.8 | 48.7 | 38.5
| TSI | 2.9 | 21.6 | 75.5
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19340012
|Trait=Tanning
|Title=Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry
|RiskAllele=C
|Pval=7E-8
|OA=1
}}

{{PMID Auto
|PMID=18076761
|Title=In silico and in vitro comparative analysis to select, validate and test SNPs for human identification.
|OA=1
}}

{{PMID Auto
|PMID=19366436
|Title=Whole genome amplification and real-time PCR in forensic casework.
|OA=1
}}

{{PMID Auto
|PMID=20585627
|Title=Web-based, participant-driven studies yield novel genetic associations for common traits.
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs154659
|overall_frequency_n=48
|overall_frequency_d=128
|overall_frequency=0.375
|n_genomes=34
|n_genomes_annotated=0
|n_haplomes=44
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|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 | HumanOmni1Quad}}
{{on chip | Illumina Human 1M}}