Variant annotations

Available GET parameters:

add-all-data = 1 or 0 
add-region-databases = 1 or 0 
expand-pubmed-articles = 1 or 0 
add-main-data-points = 1 or 0 
add-source-databases = all or none or refseq-transcripts,ensembl-transcripts,sanger-cosmic-licensed,iarc-tp53-germline,wustl-civic,isb-kaviar3,gwas,sanger-cosmic,thousand-genomes,dann-snvs,ncbi-clinvar2,weill-cornell-medicine-pmkb,dbnsfp-dbscsnv,gnomad-exomes-coverage,uniprot-variants,gnomad-genomes-coverage,dbnsfp,gnomad-exomes,icgc-somatic,ncbi-dbsnp,sanger-cosmic-public,iarc-tp53-somatic,broad-exac,gerp,gnomad-genomes 
allele-frequency-threshold = float 
add-ACMG-annotation = 1 or 0 
minimum-clinvar-stars = 0 or 1 or 2 or 3 or 4 
exclude-source-databases = refseq-transcripts,ensembl-transcripts,sanger-cosmic-licensed,iarc-tp53-germline,wustl-civic,isb-kaviar3,gwas,sanger-cosmic,thousand-genomes,dann-snvs,ncbi-clinvar2,weill-cornell-medicine-pmkb,dbnsfp-dbscsnv,gnomad-exomes-coverage,uniprot-variants,gnomad-genomes-coverage,dbnsfp,gnomad-exomes,icgc-somatic,ncbi-dbsnp,sanger-cosmic-public,iarc-tp53-somatic,broad-exac,gerp,gnomad-genomes
GET /lookup/chr19:20082943:1:G?format=api
HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Cache-Control: max-age=0
Content-Type: application/json
ETag: "1c1a21de74492ee1b14888de77ac3a52"
Vary: Accept

{
    "chromosome": "chr19",
    "alt": "G",
    "ref": "T",
    "pos": 20082943,
    "variant_id": "10190190200829430003",
    "variant_type": "SNV",
    "cytobands": "19p12"
}