List of variants reported as uncertain significance for eyelid disorder by University of Washington Center for Mendelian Genomics, University of Washington

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_004360.5(CDH1):c.1198G>A (p.Asp400Asn)	rs1960893142
NM_004360.5(CDH1):c.779C>T (p.Pro260Leu)	rs1960783816

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