Traits - Motion sickness resistance

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Motion sickness resistance

Behavioral Response

Motion sickness happens when the brain receives mismatched signals from the inner ear, eyes, and body sensors.

GWAS work has identified more than 30 variants linked to motion sickness susceptibility, with some overlap with migraine and balance traits.

This result reflects research-level variation in motion-sickness biology and is not a clinical evaluation.

Age, pregnancy, type of motion (car, sea, air), reading or screens during travel, dehydration, and medications all strongly affect actual motion sickness.

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Report markers
35 SNP entries
Genes
0
Research
1 study
Your report

Genetic tendency

Average genetic tendency

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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
rs4076764TC64.90%
rs4343996GA45.10%
rs56051278GGG26.50%
rs61759167TTT23.10%
rs62018380CAA86.90%
rs66800491GAA68.30%
rs6946969GAA65.80%
rs705145CA63.80%
rs10970305ACC50.50%
rs11713169ACC16.00%
rs149951341CA79.80%
rs1782032GGG54.40%
rs1858111GA56.70%
rs2150864GA34.80%
rs2360806ACC16.20%
rs34912216GAA72.70%
rs10514168--A85.40%
rs10752212--A53.20%
rs60464047--A85.00%
rs6069325--G84.10%
rs6833641--85.20%
rs7170668--63.20%
rs7957589--T14.60%
rs9834560--61.00%
rs9906289--T4.60%
rs997295--T58.80%
rs11129078--A75.10%
rs1195218--91.60%
rs1378552--T32.20%
rs17515225--44.50%
rs1847202--C64.40%
rs2153535--G48.00%
rs2318131--C34.30%
rs2551802--G69.70%
rs34311235--T36.80%

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: 16/35 SNP entries detected (45%).

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

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