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Original Research

Association between heterozygote Val92Met MC1R gene polymorphisms with incidence of melasma: a study of Javanese women population in Yogyakarta

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Pages 489-495 | Published online: 02 Jul 2019

Figures & data

Table 1 Characteristics of age, sun exposures, and family history of the two groups: with melasma and without melasma (n=158)

Figure 1 Sequencing results of the heterozygote Val92Met genotype of the MC1R gene polymorphisms.

Notes: The MC1R Val92Met polymorphism involved amino acid substitution from Valine to Methonine at codon 92. (A) Wild-type (homozygote) for the Val/Val genotype (Valine/Valine-GG). (B) Homozygote mutant for Met/Met genotype (Methionine/Methionine-AA). (C) Heterozygote variant for the Val/Met genotype (Valine/methionine-GA).
Figure 1 Sequencing results of the heterozygote Val92Met genotype of the MC1R gene polymorphisms.

Figure 2 Sequencing results of the heterozygote Arg163Gln genotype of the MC1R gene polymorphisms.

Notes: The MC1R Arg163 Gln polymorphism involved amino acid substitution from Arginine to Glutamine at codon 163. (A) Wild-type (homozygote) for the Arg/Arg genotype (Arginine/Arginine-GG). (B) Homozygote mutant for the Gln/Gln genotype (Glutamine/Glutamine-AA). (C) Heterozygote variant for the Arg/Gln genotype (Arginine/Glutamine-GA).
Figure 2 Sequencing results of the heterozygote Arg163Gln genotype of the MC1R gene polymorphisms.

Table 2 Association between Val92Met and Arg163Gln genotypes of MC1R gene polymorphisms and melasma