GA4GH Beacon v2 Explorer
Federated genomic variant discovery API and interactive explorer for Enigma Clinical Platform (ECP) with Saudi PDPL small-cell privacy suppression.
- GA4GH v2.0.0
- Beacon Specification
- GRCh38 / hg38
- Genome Assembly
- Saudi PDPL (k=5)
- Privacy Standard
- 3 Active Routes
- Federated Endpoints
Sovereign Privacy Compliance & Small-Cell K-Anonymity (Saudi PDPL)
Enigma Clinical Platform (ECP) implements the international GA4GH Beacon v2.0.0 protocol under the regulatory framework of the Saudi Personal Data Protection Law (PDPL). To eliminate any re-identification risks for individuals harboring ultra-rare variants, queries returning fewer than 5 alleles (1 ≤ AC < 5) return exists: true for federated discovery but suppress exact counts and frequencies.
Interactive Presets
Select a curated benchmark variant to test boolean discovery, exact cohort counts, or small-cell privacy suppression.
Genomic Variant Query Builder
Search for sequence-resolved alleles and short variations in the Enigma Clinical Platform (ECP) GRCh38 exome cohort.
Production Beacon v2 Endpoints
Standard GA4GH Beacon v2 REST API contracts hosted at clinical.enigmagenomics.com.
/api/beacon/v2/infoReturns institutional metadata, welcome URLs, supported GA4GH Beacon v2 specifications, open-access datasets, and sovereign governance terms.
/api/beacon/v2/g_variantsGenomic variant discovery query. Supports assemblyId, referenceName, start, referenceBases, alternateBases, and requestedGranularity (boolean, count, record). Enforces Saudi PDPL privacy.
/api/beacon/v2/filtering_termsReturns supported alphanumeric and ontology filtering terms across Human Phenotype Ontology (HPO), MONDO, ClinVar, ACMG/AMP criteria, and Sequence Ontology.
Ontology & Alphanumeric Filtering Terms
Beacon v2 filtering terms supported by Enigma Clinical Platform (ECP) for phenotypic and clinical variant stratification.
| Term Identifier | Label / Description | Category | Type | Applicable Scopes |
|---|---|---|---|---|
HP:0001250 | Seizures | HPO | ontology | individuals biosamples |
HP:0001249 | Intellectual disability | HPO | ontology | individuals biosamples |
HP:0000252 | Microcephaly | HPO | ontology | individuals biosamples |
HP:0001257 | Spasticity | HPO | ontology | individuals biosamples |
HP:0001627 | Abnormal heart morphology | HPO | ontology | individuals biosamples |
| Term Identifier | Label / Description | Category | Type | Applicable Scopes |
|---|---|---|---|---|
HP:0001250 | Seizures | HPO | ontology | individuals biosamples |
HP:0001249 | Intellectual disability | HPO | ontology | individuals biosamples |
HP:0000252 | Microcephaly | HPO | ontology | individuals biosamples |
HP:0001257 | Spasticity | HPO | ontology | individuals biosamples |
HP:0001627 | Abnormal heart morphology | HPO | ontology | individuals biosamples |
HP:0000007 | Autosomal recessive inheritance | HPO | ontology | individuals biosamples |
HP:0001518 | Small stature / growth restriction | HPO | ontology | individuals biosamples |
HP:0000505 | Visual impairment | HPO | ontology | individuals biosamples |
HP:0000365 | Hearing impairment | HPO | ontology | individuals biosamples |
HP:0002011 | Morphological abnormality of central nervous system | HPO | ontology | individuals biosamples |
MONDO:0000508 | Mendelian disease | MONDO | ontology | individuals biosamples |
MONDO:0005044 | Sickle cell anemia | MONDO | ontology | individuals biosamples |
MONDO:0009688 | Meckel syndrome | MONDO | ontology | individuals biosamples |
MONDO:0011571 | Sanjad-Sakati syndrome | MONDO | ontology | individuals biosamples |
MONDO:0009061 | Cystic fibrosis | MONDO | ontology | individuals biosamples |
MONDO:0019052 | Inborn errors of metabolism | MONDO | ontology | individuals biosamples |
MONDO:0007254 | Hereditary breast ovarian cancer syndrome | MONDO | ontology | individuals biosamples |
MONDO:0005041 | Familial hypercholesterolemia | MONDO | ontology | individuals biosamples |
ClinVar:Pathogenic | Pathogenic | ClinVar | alphanumeric | g_variants |
ClinVar:Likely_pathogenic | Likely Pathogenic | ClinVar | alphanumeric | g_variants |
ClinVar:VUS | Variant of Uncertain Significance | ClinVar | alphanumeric | g_variants |
ClinVar:Likely_benign | Likely Benign | ClinVar | alphanumeric | g_variants |
ClinVar:Benign | Benign | ClinVar | alphanumeric | g_variants |
ACMG:PVS1 | Null variant in gene where loss of function is known disease mechanism | ACMG | alphanumeric | g_variants |
ACMG:PS1 | Same amino acid change as established pathogenic variant | ACMG | alphanumeric | g_variants |
ACMG:PM2 | Absent or extremely rare in population databases | ACMG | alphanumeric | g_variants |
ACMG:PP3 | Multiple lines of in silico computational evidence predict damaging effect | ACMG | alphanumeric | g_variants |
ACMG:BA1 | Allele frequency above 5% in population databases (Stand-Alone Benign) | ACMG | alphanumeric | g_variants |
ACMG:BS1 | Allele frequency greater than expected for disorder | ACMG | alphanumeric | g_variants |
SO:0001587 | stop_gained (nonsense) | Consequence | ontology | g_variants |
SO:0001589 | frameshift_variant | Consequence | ontology | g_variants |
SO:0001575 | splice_donor_variant | Consequence | ontology | g_variants |
SO:0001574 | splice_acceptor_variant | Consequence | ontology | g_variants |
SO:0001583 | missense_variant | Consequence | ontology | g_variants |
SO:0001819 | synonymous_variant | Consequence | ontology | g_variants |
ECP:homozygous | Homozygous state observed in cohort | Zygosity | custom | g_variants individuals |
ECP:heterozygous | Heterozygous carrier state observed in cohort | Zygosity | custom | g_variants individuals |
ECP:founder_variant | Verified founder mutation in cohort | Zygosity | custom | g_variants |