dbSNP Reference SNP number (rsID)
ID dbsnp_id
DatatypeNot PIIidentifierDraft
This record is a draft: it has not been reviewed yet and may be incomplete or wrong. Do not rely on it for compliance decisions. Help improve it (see CONTRIBUTING.md).
Identifier of a reference SNP record (RefSNP) in dbSNP, the database of short genetic variations kept by the US National Center for Biotechnology Information (NCBI). It is the letters rs followed by a number. A RefSNP groups the submitted reports of a variant at the same location of the reference genome, so genome-wide association studies, genotyping files and variant annotations use the rsID to name a variant.
- Categories
- Scientific, Medical/pharma identifiers
- Countries
- Global (not tied to a country)
- Languages
- Common to most languages
- AutoType benchmark
SNPID_correct- Bioregistry
dbsnp- Wikidata
- P6861
- Quality
- 100/100
- Metacrafter rules
- no detection rule yet
- Supported by tools
- Auto-Type
Regular expression
^rs[1-9]\d*$Python re syntax.
Examples
| Value | Description |
|---|---|
| rs334 | Variant of the HBB gene behind sickle cell disease |
| rs113488022 | Example of Wikidata property P6861 |
| rs121913355 | Example of Wikidata property P6861 |
| ss334 invalid | Submitted SNP (ss) number, not a RefSNP |
Translations
| Language | Name | Description |
|---|---|---|
| Russian | Идентификатор варианта dbSNP (rsID) | Номер записи RefSNP в базе генетических вариаций dbSNP (NCBI): буквы rs и число. |
Sources
- wikipedia: https://en.wikipedia.org/wiki/DbSNP
- wikidata: https://www.wikidata.org/wiki/Property:P6861
- doc: https://www.ncbi.nlm.nih.gov/snp/docs/RefSNP_about/
- other: https://github.com/congy/AutoType/blob/master/data_release/SNPID_correct.txt
Use this record
- Page URL:
http://registry.apicrafter.io/datatype/dbsnp_id - JSON: API v1 · legacy shape (used by metacrafter) · Markdown (for LLMs)
- Improve it: edit
data/datatypes/any/science/dbsnp_id.yamlon GitHub