Related gene-specific medical variations for Gene (Select 142891) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2640609	NM_001007271.3(DUSP13A):c.18C>G (p.Leu6=)	DUSP13A, DUSP13B +1 more	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 786165	NM_001007273.2(DUSP13B):c.143C>T (p.Ala48Val)	DUSP13B, SAMD8 (A48V)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 780870	NM_001007273.2(DUSP13B):c.105C>T (p.Val35=)	DUSP13B, SAMD8	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign

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