Overview
Comprehensive genetic analysis of your risk of Malignant Hyperthermia
Malignant hyperthermia can cause sudden death when a person is exposed to certain types of anesthesia, such as anesthesia commonly used during surgery.
Death from Malignant Hyperthermia is entirely preventable as long as the anesthesiologist knows the person is at risk before the person is given anesthesia.
This app empowers you with a straightforward analysis of genes known to be associated with Malignant Hyperthermia or Central Core Disease (a condition similar to Malignant Hyperthermia). You'll receive a genetic report that includes the results of the analysis as well as actionable information you can use to help protect your wellness and longevity.
Getting Started
This app is compatible with most DNA tests including 23andMe, AncestryDNA, and MyHeritage.
Simply upload your DNA data to use this app. If you haven't yet taken a DNA test, order one of our DNA tests.
Once your DNA data is stored in your Sequencing.com account, click the app's 'Start' button. You'll receive your results in about 15 minutes.


More Ways To Learn About Your DNA
Sequencing's new DNA Education Center is your resource for learning about genome sequencing, precision medicine, and DNA discoveries. For example, you can learn about how genetic testing for diseases works.
For captivating stories about DNA in recent news, The Sequencing Blog provides you with weekly interesting insights.
Free DNA Data Upload
This app can analyze DNA data from almost all genetic tests and genome sequencing services.
Test Compatibility | Format Compatibility | Variant Compatibility | Reference Genome Compatibility | |||
---|---|---|---|---|---|---|
Whole Genome Sequencing | FASTQ and FQ | SNP / SNV (Single Nucleotide Variants) |
hg38 / GRCh38 | |||
Exome Sequencing | FASTA and FA | hg19 / GRCh37 | ||||
Ultimate DNA Test | BAM | hg18 / GRCh36 | ||||
23andMe | SAM | hg17 / GRCh35 | ||||
AncestryDNA | CRAM | |||||
MyHeritage | VCF | |||||
Dante Labs | Genome VCF (gVCF and GVCF) | |||||
Nebula Genomics | TXT | |||||
Genes for Good | CSV | |||||
Living DNA | TAB | |||||
HomeDNA | gz and zip compressed files | |||||
FTDNA | almost all other genetic data formats | |||||
Silverberry Genomix | ||||||
Toolbox Genomics | ||||||
Full Genomes | ||||||
Color | ||||||
New Amsterdam Genomics | ||||||
24Genetics | ||||||
Vitagene | ||||||
Helix | ||||||
Genos | ||||||
tellmeGen | ||||||
GSA | ||||||
Axiom | ||||||
almost all other genetic tests |
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Disclaimer
The genetic analysis and statements that appear in this app and report have not been evaluated by the United States Food and Drug Administration. The Sequencing.com website and all software applications (Apps) that use Sequencing.com's website, as well as Sequencing.com's open Application Programming Interface (API), are not intended to diagnose, monitor, treat, cure, prevent nor alleviate any disease.
While this DNA analysis app can analyze data from many different types of genetic tests, it is important to take into consideration that the data from some types of genetic tests may not provide a complete assessment of your genetic risk of malignant hyperthermia. For example, if your DNA data is from a genotyping genetic test, which is the type of testing used by 23andMe, AncestryDNA, MyHeritage, FamilyTreeDNA, and Living DNA, then the analysis of your DNA data and the report provided by this app may not give you a complete understanding of your genetic risk of malignant hyperthermia, especially if malignant hyperthermia runs in your family.
If you think you may be at higher risk for malignant hyperthermia, it is best to work with a doctor or genetic counselor who can assess your risk, interpret your results, and build an action plan.
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