This is an example of merged JSON documents for variant annotations (actual data may not be accurate)

merged_variant_json_doc

{
    "_id": "15:g.33905410A>G",
    "mutdb": {
        "chromEnd": 33905410,
        "dbsnp_id": "rs2229116",
        "allele2": "G",
        "uniprot_id": "VAR_011405",
        "allele1": "A",
        "mutpred_score": 0.384,
        "cosmic_id": null,
        "chromStart": 33905410,
        "chrom": "15",
        "strand": "p"
    },
    "dbsnp": {
        "chromEnd": 33905410,
        "snpclass": "single",
        "allele2": "G",
        "allele1": "A",
        "rsid": "rs2229116",
        "func": "missense",
        "chromStart": 33905409,
        "chrom": "15",
        "strand": "+"
    },
    "cosmic": {
        "chromEnd": 33905410,
        "allele2": "G",
        "allele1": "A",
        "mut_freq": ".9",
        "chromStart": 33905410,
        "chrom": "15",
        "mut_nt": "A>G",
        "tumor_site": "large_intestine"
    },
    "gwassnps": {
        "chromEnd": 33905410,
        "allele2": "G",
        "trait": "A genome-wide association study of carotid atherosclerosis in HIV-infected men.",
        "allele1": "A",
        "pubmedID": 20009918,
        "rsid": "rs2229116",
        "chromStart": 33905409,
        "chrom": "15"
    }
}