dbSNP

Foundational archive for single nucleotide polymorphisms and multiple small-scale variations.

What it does

The critical backbone for rsID variant identification, linking global population frequency studies back to the NCBI framework.

How to use

See https://www.ncbi.nlm.nih.gov/snp/ for documentation and access.

STRC usage

PARTIAL — API returned reference mismatch error for E1659A. May need different query format. rsID not yet assigned to this variant.

Connections

• STRC Variant c.4976A>C — Misha [see-also]
• STRC Gene [about]
• [part-of] Tools index