"Genome-Nilou Lab"[submitter] AND "MADD"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1243998	NM_001376571.1(MADD):c.1041G>A (p.Glu347=)	MADD	Single nucleotide variant (synonymous variant +1 more)	Deeah syndrome +2 more	GBenign
Select item 1321156	NM_001376571.1(MADD):c.1440T>C (p.Asn480=)	MADD	Single nucleotide variant (synonymous variant +1 more)	not provided +2 more	GBenign
Select item 1321157	NM_001376571.1(MADD):c.2294G>A (p.Arg765Gln)	MADD (R543Q +2 more)	Single nucleotide variant (missense variant +2 more)	not provided +2 more	GBenign

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