Variant: rs1129038

present in Gene: HERC2 present in Chromosome: 15 Position on Chromosome: 28111713 Alleles of this Variant: C/T

rs1129038 in HERC2 gene and Astigmatism PMID 30306274 2018 Genome-wide association studies for corneal and refractive astigmatism in UK Biobank demonstrate a shared role for myopia susceptibility loci.

rs1129038 in HERC2 gene and Eye Color PMID 23486544 2013 Genetics of eye colours in different rural populations on the Silk Road.

rs1129038 in HERC2 gene and Hair Color PMID 30531825 2018 Genome-wide study of hair colour in UK Biobank explains most of the SNP heritability.

rs1129038 in HERC2 gene and Regular astigmatism - corneal PMID 30306274 2018 Genome-wide association studies for corneal and refractive astigmatism in UK Biobank demonstrate a shared role for myopia susceptibility loci.

rs1129038 in HERC2 gene and Skin Pigmentation PMID 30166351 2018 Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort.

rs1129038 in HERC2 gene and Suntan PMID 30166351 2018 Multitrait genome association analysis identifies new susceptibility genes for human anthropometric variation in the GCAT cohort.

rs1129038 in HERC2 gene and Vitiligo PMID 22561518 2012 Genome-wide association analyses identify 13 new susceptibility loci for generalized vitiligo.

rs1129038 in HERC2 gene and melanoma PMID 21926416 2011 Genome-wide association study identifies novel loci predisposing to cutaneous melanoma.