> For the complete documentation index, see [llms.txt](https://help.connected.illumina.com/llms.txt). Markdown versions of documentation pages are available by appending `.md` to page URLs; this page is available as [Markdown](https://help.connected.illumina.com/emedgene/emedgene-analyze-manual/reviewing_a_case/candidates-tab/most_likely_candidates_and_candidates.md).

# Most Likely Candidates and Candidates

To streamline case review, the **AI Shortlist** pre-selects the list of variants likely to be causative for each case: **Most Likely Candidates** and **Candidates**.

### **Most Likely Candidates**

Variants that are most promising for solving the case. This list is limited to 10 top-scored variants but may include more if more than one variant is tagged per gene (suggesting compound heterozygosity). We can change the **Most Likely Candidates** number limit upon request.

### **Candidates**

Several dozen highly scored variants worth considering.

The ranking of variants by **AI Shortlist** considers:

* SNVs
* CNVs
* SNV + CNV compound heterozygotes
* SVs
* mtDNA variants
* STRs

The **AI Shortlist** rates variants based on predicted variant effects, alternative allele frequency, familial segregation pattern, phenotypic match, in silico predictions, and other relevant information from scientific papers and databases.

During the case review, you can untag variants selected by the **AI Shortlist** or manually tag ones not selected by the **AI Shortlist**.


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