Traits - Smell sensitivity

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Smell sensitivity

Taste & Smell

Smell sensitivity covers research on inherited differences in how strongly people detect a wide range of odors.

GWAS work has identified variants in olfactory receptor genes that influence detection thresholds for specific compounds.

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

Age, smoking, head injury, recent illness (including viral infections), nasal health, and exposure history all strongly affect real smell sensitivity.

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Report markers
15 SNP entries
Genes
0
Research
1 study
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Genetic tendency

Average genetic tendency

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Explore the evidence

Behind this report

Review the genes, tested markers and supporting research.

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
rs12291225CAA25.00%
rs2075650AG13.00%
rs2251885AG37.00%
rs6052484GAA26.00%
rs11174650--T8.00%
rs16875528--C1.00%
rs17252438--5.00%
rs199443--T20.00%
rs2732614--T20.00%
rs3751196--A6.00%
rs4111--C15.00%
rs4715057--G2.00%
rs4865875--9.00%
rs605843--25.00%
rs9321099--A9.00%

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.

2015 Nov Medicine (Baltimore)

Authors: Dong J, Yang J, Tranah G, Franceschini N, Parimi N, Alkorta-Aranburu G, Xu Z, Alonso A, Cummings SR, Fornage M, Huang X, Kritchevsky S, Liu Y, London S, Niu L, Wilson RS, De Jager PL, Yu L, Singleton AB, Harris T, Mosley TH, Pinto JM, Bennett DA, Chen H

Study sample: 6,252 individuals (european ancestry)

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Coverage: 4/15 SNP entries detected (26%).

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

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