Thursday, 01 10th

Last updateTue, 30 Aug 2016 11am


FINDbase design allows storing and retrieval of causative mutation and pharmacogenomic markers allele frequencies data in various population and ethnic groups worldwide. These data are available for research use only in the fields of human population genetics and molecular genetics.
We are fully aware that genetic, like historical and biological, data can be misused for stigmatization and discrimination against certain ethnic groups, or individuals and as such the use of the allele frequency data stored in FINDbase for such purposes would not be ethically or scientifically justified. In addition, FINDbase contains allele frequencies calculated on a summary level, and as such any personal information that would lead to individual identification, is removed.

By entering FINDbase, you agree that you will not use the data to discriminate or stigmatize any population or ethnic group.

About us

As molecular genetic testing and electronic healthcare records become increasingly common features of modern medical practice, there is a need to integrate information in genetic databases to establish a detailed understanding of how genome sequence differences impact on human health.

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  • Add: 2, Stone Buildings, Lincoln's Inn, London WC2A 3TH, United Kingdom
  • Tel: +44-(0)207-608.51.91
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