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. 2006 Nov 28;35(Database issue):D690–D695. doi: 10.1093/nar/gkl934

Figure 2.

Figure 2

Querying FINDbase for frequencies of mutations leading to a certain inherited disorder in different populations. (a) Construction of the query ‘Find frequent (between 2 and 100%) familial hypercholesterolemia mutations in all populations’. (b) The user needs to select for the ‘Familiar hypercholesterolemia’ disorder from the disorder's menu, located either in the Home page [next to the world map (Supplementary Figure)] or at the right part of the Search page. Query results are in a table format, indicating the populations and ethnic groups (if applicable) where LDLR mutations are found. Information is accompanied by the data source. (c) Construction of the query ‘Find the frequency of the p.S188F mutation leading to Glucose 6P-Dehydrogenase (G6PD) deficiency in all populations’. By selecting ‘Glucose 6P-Dehydrogenase deficiency’ from the disorder's list and ‘p.S188F’ from the mutation's list, the query returns a list of populations in which the p.S188F mutation is found together with the corresponding frequencies. Query output can be in a graphical (d) or table format (e), always accompanied by the data source.