List of variants reported as uncertain significance for hereditary skin disorder by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_002461.3(MVD):c.70+5G>A	rs200035262	0.00306
NM_020638.3(FGF23):c.211A>G (p.Ser71Gly)	rs104894342	0.00001
NM_006846.4(SPINK5):c.2740-127_2740-126del	rs797045108

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