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Enigma ClinicalPlatform

الرئيسية البيانات أمثلة البحث المصادر الأسئلة الشائعة اتصل بنا

تقديم البيانات

Enigma ClinicalPlatform

Genomic evidence for variant interpretation and discovery.

Enigma Clinical v1 · GRCh38

Explore

Home
Data
Search examples
Resources
FAQ
Contact
Submit data

Resources

Rare diseases
Clinical trials
Carrier screening panel
Example searches
Batch variant search
Liftover (hg38 / b37 / hg19)
Pedigree tree builder
Clinical reasoning copilot
PGx diplotype translator
My panels and saved searches
Cohort insights
Mitochondrial & Y haplogroups
3D Protein structure viewer (Mol*)
Homozygous LoF registry
ClinVar discordance alerts
Founder variant registry
Germline classification
Somatic classification
SV implementation
Data sources
Data access & e-DUA
Cite the platform
GA4GH Beacon v2
API for developers
About

Contact

sgp-support@enigmagenomics.com
sgp-data@enigmagenomics.com
Privacy & data protection

Data sources

gnomAD v4
ClinVar
GENCODE / Ensembl
MANE
Ensembl VEP
GTEx
Human Phenotype Ontology
Franklin by Genoox
GeneBe

For research use. Classifications are reproduced from their source databases and are not a substitute for clinical interpretation.

© 2026 Enigma Clinical · Built by Enigma Genomics