List of variants reported as uncertain significance for hereditary epidermal appendage anomaly by Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001039570.3(KREMEN1):c.121G>C (p.Asp41His)
NM_001039570.3(KREMEN1):c.1351G>A (p.Asp451Asn)
NM_025132.4(WDR19):c.[291-21A>G];[542C>G]

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