CLINVAR DATABASE

Variant Lookup

Instantly decode RSIDs and HGVS notations using the world's most trusted genetic variant archive.

Educational only. Not medical advice. Consult a healthcare provider for personalized guidance.
Genomic Variant Lookup
ClinVar_Realtime_Access_Engine

Accepted_Identifier_Protocols

  • dbSNP Referencers1234567
  • HGVS StandardNM_000123.4:c.123A>G
  • ClinVar IDVCV000012345
About ClinVar

ClinVar is a freely accessible, public archive of reports on the relationships among human variations and phenotypes, hosted by the National Center for Biotechnology Information (NCBI).

It serves as a critical resource for determining whether a specific genetic variant has been linked to disease in clinical studies.

Classification Guide
PathogenicStrong evidence causes disease
Uncertain Significance (VUS)Insufficient evidence to classify
BenignStrong evidence it is harmless