C1832370[trait identifier] AND "Genome-Nilou Lab"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 36002	NM_001927.4(DES):c.75A>G (p.Pro25=)	DES	Single nucleotide variant (synonymous variant)	Desmin-related myofibrillar myopathy +7 more	GBenign
Select item 36003	NM_001927.4(DES):c.93T>C (p.Ser31=)	DES	Single nucleotide variant (synonymous variant)	not specified +7 more	GBenign
Select item 258491	NM_001927.4(DES):c.579-38C>T	DES	Single nucleotide variant (intron variant)	not provided +4 more	GBenign

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