pharmgkb.variant_lookup

mock data$0.001 / call

PharmGKB Variant Lookup

Look up pharmacogenomic details for a genetic variant by dbSNP rsID (e.g. rs1799853 for CYP2C9*2, rs4244285 for CYP2C19*2, rs12248560 for CYP2C19*17). Returns variant ID, change classification (Missense/Synonymous/Intronic), clinical significance (drug-response/pathogenic), variant type (SNP/Indel), chromosomal position (GRCh38), associated genes, rarity flag, and ClinVar IDs. Focused on variants with known drug-response relevance. Source: PharmGKB, CC BY-SA 4.0.

Healthprovider: Pharmgkb#pharmgkb#health

Input schema

rsidrequired

dbSNP reference SNP ID for the variant (e.g. rs1799853, rs4244285, rs12248560). Must be prefixed with "rs" followed by digits. PharmGKB annotates variants with known pharmacogenomic relevance.

string

Call via REST

curl -X POST https://unifyapi.pro/api/call/pharmgkb.variant_lookup \
  -H "Authorization: Bearer uak_live_..." \
  -H "Content-Type: application/json" \
  -d '{"rsid":"<rsid>"}'

Try it

Paste a UnifyAPI key (create one in the dashboard) and run a real call.

API key

rsid *