Traits - Sweetness detection

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Sweetness detection

Taste & Smell

Sweetness detection covers inherited differences in how strongly sweet flavors are perceived on the tongue.

Variants in the sweet taste receptor genes (TAS1R2 and TAS1R3) have been linked to differences in sweet perception.

This result reflects research-level variation in taste biology and is not a clinical taste test.

Diet, age, smoking, oral health, and food culture also strongly affect how sweetness is perceived in everyday eating.

Selected sample
Demo Report
Report markers
3 SNP entries
Genes
1
Research
1 study
Your report

Genetic tendency

Average ability to detect sweetness

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Explore the evidence

Behind this report

Review the genes, tested markers and supporting research.

Genes analyzed

Gene summaries include genomic locations and associated markers. A detected genotype does not by itself indicate a health condition.

Understanding the data
SNP
A specific genetic marker relevant to this trait.
Genotype
The DNA letters reported at a marker location.
Variant allele
The alternative DNA sequence at the SNP site.
Variant allele frequency
The reported percentage of the reference population carrying this variant.
Variant found
Whether the variant was detected in your DNA file.

1 of 1 genes have detected genotypes.

TAS1R3

The protein encoded by this gene is a G-protein coupled receptor involved in taste responses. The encoded protein can form a heterodimeric receptor with TAS1R1 to elicit the umami taste response, or it can bind with TAS1R2 to form a receptor for the sweet taste response. [provided by RefSeq, Nov 2015]

GeneCards
Chromosome
1
Start
1,331,280
End
1,335,320
Build
HG19
Associated SNPs 1 / 1 detected
Associated markers for TAS1R3
SNPGenotype Ref. alleleVariant alleleFrequencyStatus
rs35744813 CC TC71.57%Detected

SNPs tested

These are the unique genetic markers analyzed for this trait. Genotypes showing "--" were not identified in your DNA file. Report marker totals can include repeated study entries; this table shows each SNP once.

Genotypes and reported variant frequencies
SNPChromosomeGenotypeVariant alleleFrequency
rs357448131CCC71.57%

DNA Genics reports genotypes based on the 'positive' strand of the human genome reference sequence (build 37/HG19). Other companies may use the opposite strand, so genotypes may need conversion for comparison.

Research studies

The following peer-reviewed scientific studies support the genetic associations analyzed in this report.

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Coverage: 3/3 SNP entries detected (100%).

Reference: Human Genome Build 37 (HG19). Other testing companies may report using the opposite strand, requiring conversion for comparison.

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SAMPLE REPORT Example DNA profile This is a sample report with example data. It is not your personal report, and the results do not describe you.
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