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|
In genetics, rs16891982, also known as F37 … In genetics, rs16891982, also known as F374L, is the name for a single nucleotide polymorphism found in the SLC45A2 gene. The SNP consists of two alleles: C (cytosine) and G (guanine).It is associated with skin tone and hair/eye color. It is a type of missense mutation. C allele homozygosity is associated with black hair in people of European descent, although those with this genotype are usually of non-European descent. C/G allele heterozygosity is associated with black hair in people of European descent G allele homozygosity is associated with light skin, hair, and eye color (European ancestry), those with this genotype also have a slightly higher susceptibility to melanoma.lightly higher susceptibility to melanoma.
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71886846
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2988
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1115011019
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, http://dbpedia.org/resource/SLC45A2 +
, http://dbpedia.org/resource/Missense_mutation +
, http://dbpedia.org/resource/Melanoma +
, http://dbpedia.org/resource/Category:SNPs_on_chromosome_5 +
, http://dbpedia.org/resource/Guanine +
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5
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http://dbpedia.org/resource/SLC45A2 +
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c.1122C>G
, F374L
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Exon 5
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rs16891982
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| rdfs:comment |
In genetics, rs16891982, also known as F37 … In genetics, rs16891982, also known as F374L, is the name for a single nucleotide polymorphism found in the SLC45A2 gene. The SNP consists of two alleles: C (cytosine) and G (guanine).It is associated with skin tone and hair/eye color. It is a type of missense mutation. C allele homozygosity is associated with black hair in people of European descent, although those with this genotype are usually of non-European descent. C/G allele heterozygosity is associated with black hair in people of European descenth black hair in people of European descent
|
| rdfs:label |
Rs16891982
|
