Variant: rs1042602 

    present in Gene: LOC107984363;TYR
    present in Chromosome: 11
    Position on Chromosome: 89178528
    Alleles of this Variant: C/A

rs1042602 in LOC107984363;TYR gene and Freckles PMID 17952075 2007 Genetic determinants of hair, eye and skin pigmentation in Europeans.

rs1042602 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.

rs1042602 in LOC107984363;TYR gene and Melanosis PMID 17952075 2007 Genetic determinants of hair, eye and skin pigmentation in Europeans.

rs1042602 in LOC107984363;TYR gene and Skin Pigmentation PMID 30166351 2018 Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort.

PMID 17999355 2007 A genomewide association study of skin pigmentation in a South Asian population.

rs1042602 in LOC107984363;TYR gene and Tonometry PMID 29617998 2018 Genome-wide association analyses identify new loci influencing intraocular pressure.