List of variants reported as uncertain significance for Amelocerebrohypohidrotic syndrome by New York Genome Center

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_024589.3(ROGDI):c.859T>C (p.Phe287Leu)	rs149138180	0.00036
NM_024589.3(ROGDI):c.691A>G (p.Met231Val)	rs137934107	0.00011
NM_024589.3(ROGDI):c.755C>G (p.Pro252Arg)	rs1276539581	0.00001
NM_024589.3(ROGDI):c.658G>T (p.Ala220Ser)	rs546063670

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