{{Rsnum
|rsid=12210050
|Chromosome=6
|position=475489
|Orientation=plus
|GMAF=0.06015
|Assembly=GRCh37
|GenomeBuild=37.1
|dbSNPBuild=131
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
}}
{{PMID|24270849|OA=1
}} [[rs12210050]] was found to be associated with [[basal cell carcinoma]] based on a study by the eMERGE network in which electronic medical records were searched to find clinical associations associated with selected SNPs.
{{ population diversity
| geno1=(C;C)
| geno2=(C;T)
| geno3=(T;T)
| CEU | 69.9 | 28.3 | 1.8
| HCB | 100.0 | 0.0 | 0.0
| JPT | 100.0 | 0.0 | 0.0
| YRI | 98.6 | 1.4 | 0.0
| ASW | 93.0 | 5.3 | 1.8
| CHB | 100.0 | 0.0 | 0.0
| CHD | 0.0 | 0.0 | 0.0
| GIH | 98.0 | 2.0 | 0.0
| LWK | 0.0 | 0.0 | 0.0
| MEX | 94.8 | 5.2 | 0.0
| MKK | 0.0 | 0.0 | 0.0
| TSI | 82.4 | 17.6 | 0.0
| HapMapRevision=28
}}{{PMID Auto GWAS
|PMID=19340012
|Trait=Tanning
|Title=Genome-Wide Association Study of Tanning Phenotype in a Population of European Ancestry
|RiskAllele=T
|Pval=5E-14
|OA=1
}}

{{PMID Auto
|PMID=21700618
|Title=Genome-wide association study identifies novel alleles associated with risk of cutaneous basal cell carcinoma and squamous cell carcinoma
|OA=1
}}

{{GET Evidence
|impact=pathogenic
|qualified_impact=Insufficiently evaluated pathogenic
|inheritance=unknown
|quality_scores=Array
|dbsnp_id=rs12210050
|overall_frequency_n=8
|overall_frequency_d=128
|overall_frequency=0.0625
|n_genomes=9
|n_genomes_annotated=0
|n_haplomes=9
|n_articles=0
|n_articles_annotated=0
|in_gwas=Y
|autoscore=1
|webscore=N
}}

{{PMID Auto GWAS
  |PMID=22885689
  |Trait=Schizophrenia
  |Title=Genome-wide association study of multiplex schizophrenia pedigrees.
  |RiskAllele=
  |Pval=3E-6
  |OR=1.20
  |ORtxt=[NR]
  }}

{{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}}