myvariant.search
mock data$0.001 / callSearch Genetic Variants
Search the MyVariant.info database of 450M+ annotated human genetic variants using a flexible query syntax. Query by: dbSNP rsID (e.g. "rs58991260"), gene symbol (e.g. "dbsnp.gene.symbol:BRCA1"), ClinVar clinical significance (e.g. "clinvar.rcv.clinical_significance:Pathogenic"), CADD pathogenicity score (e.g. "cadd.phred:>30"), chromosomal position range (e.g. "chrom:17 AND hg19.start:[41196312 TO 41277500]"), or disease/phenotype keywords (e.g. "clinvar.rcv.conditions.name:breast cancer"). Each hit includes chromosome, genomic position (hg19/hg38), rsID, reference/alternate alleles, CADD PHRED score, ClinVar clinical significance, gnomAD allele frequency, and predicted functional consequences (SnpEff). Data integrates ClinVar, gnomAD, CADD, dbSNP, COSMIC, CIViC, ExAC, and 30+ annotation sources.
Input schema
Variant query string. Supports: rsID (e.g. "rs58991260"), gene symbol (e.g. "dbsnp.gene.symbol:BRCA1"), CADD score filter (e.g. "cadd.phred:>20"), ClinVar significance (e.g. "clinvar.rcv.clinical_significance:Pathogenic"), chromosome position (e.g. "chrom:7 AND hg19.start:[140453000 TO 140454000]"), or disease/phenotype keywords (e.g. "clinvar.rcv.conditions.name:breast cancer").
Maximum number of variant results to return (1–50, default 10).
Comma-separated fields to return per hit. Default: dbsnp,clinvar,cadd,gnomad_exome,gnomad_genome,snpeff,vcf,chrom,hg19. Other useful fields: dbnsfp,cosmic,civic,gwassnps,hg38. Use "all" for every available annotation source.
Genome assembly for coordinate fields in results. "hg19" (GRCh37) or "hg38" (GRCh38). Defaults to hg19.
Call via REST
curl -X POST https://unifyapi.pro/api/call/myvariant.search \
-H "Authorization: Bearer uak_live_..." \
-H "Content-Type: application/json" \
-d '{"q":"<q>","size":10,"fields":"<fields>","assembly":"<assembly>"}'