Variant: rs1393350 

    present in Gene: LOC107984363;TYR
    present in Chromosome: 11
    Position on Chromosome: 89277878
    Alleles of this Variant: G/A

rs1393350 in LOC107984363;TYR gene and Eye Color PMID 20585627 2010 Web-based, participant-driven studies yield novel genetic associations for common traits.

PMID 17952075 2007 Genetic determinants of hair, eye and skin pigmentation in Europeans.

rs1393350 in LOC107984363;TYR gene and Hair Color PMID 30531825 2018 Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability.

rs1393350 in LOC107984363;TYR gene and Nasopharyngeal carcinoma PMID 20512145 2010 A genome-wide association study of nasopharyngeal carcinoma identifies three new susceptibility loci.

rs1393350 in LOC107984363;TYR gene and Suntan PMID 19340012 2009 Genome-wide association study of tanning phenotype in a population of European ancestry.

rs1393350 in LOC107984363;TYR gene and Vitiligo PMID 22561518 2012 Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.

PMID 21326295 2011 Genome-wide analysis identifies a quantitative trait locus in the MHC class II region associated with generalized vitiligo age of onset.

PMID 20410501 2010 Variant of TYR and autoimmunity susceptibility loci in generalized vitiligo.

rs1393350 in LOC107984363;TYR gene and melanoma PMID 19578364 2009 Genome-wide association study identifies three loci associated with melanoma risk.

PMID 21983787 2011 Genome-wide association study identifies three new melanoma susceptibility loci.

PMID 21706340 2012 A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q.

PMID 28212542 2017 Two-stage genome-wide association study identifies a novel susceptibility locus associated with melanoma.