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. 2020 Jan 15;10:331. doi: 10.1038/s41598-019-57335-5

Figure 1.

Figure 1

The enrollment of ClinVar pathogenic and likely pathogenic variants for curation. *Variants in genes with their phenotype in OMIM were “susceptibility to complex disease or infection”, “Non-diseases”, “provisional phenotype-gene relationship” or “Not included”.