Variation
The Variation database provides human genomic variation retrieval. Original data source of Variation database includes dbSNP, dbVar, ClinVar, etc. The main available information includes genome variation (HGVS), location, organism, population frequency, related disease, phenotype, literature, etc.
Last updated
Keyword detail
Filter
Clinical significances
keyboard_arrow_down
Source databases
keyboard_arrow_down
(HP:0030359)[Phenotype ID]
found no results.