Variation Spdi To Rsids
variation_spdi_to_rsidsLook up the dbSNP rsIDs that a SPDI allele maps to, via NCBI Variation Services. AUTHORITATIVE for the reverse direction — you have a genomic coordinate and alleles from a VCF or a pipeline and need the rsID other databases key on. SPDI is 0-BASED, unlike HGVS: "NC_000007.14:140753335:A:T" is the same variant as "NC_000007.14:g.140753336A>T".
Input Schema
| Name | Required | Description | Default |
|---|---|---|---|
| spdi | Yes | SPDI as seq_id:position:deleted:inserted, 0-based position. e.g. "NC_000007.14:140753335:A:T". |