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Variation Resources

dbSNP | NCBI
Allows users to search the SNP database at NCBI, using one of the following methods:

  • Entrez SNP
  • ID Numbers
  • Submission Info
  • Batch
  • Locus Info
  • Between Markers

Human Genome Variation Database (HGVbase) | HGBASE Consortium
The objective of the HGVbase is to provide an accurate and fully comprehensive catalog of normal human gene and genome variation.

International HapMap Project | International HapMap Project
HapMap is a catalog of common genetic variants that occur in human beings. It describes what these variants are, where they occur in our DNA, and how they are distributed among people within populations and among populations in different parts of the world.

Online Mendelian Inheritance in Man (OMIM) | Johns Hopkins University
A full text knowledgebase of human genes and genetic disorders. Each record in OMIM serves as a summary of the current state of knowledge of the gene or disorder; records may be thought of as review articles.

Mitelman Database of Chromosome Aberrations in Cancer | Mitelman F, Johansson B and Mertens F (Eds.)
Records chromosomal aberrations to tumor characteristics, based either on individual cases or associations. All the data have been manually culled from the literature by Felix Mitelman, Bertil Johansson, and Fredrik Mertens.


   
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