Related gene-specific medical variations for Gene (Select 64769) - ClinVar - NCBI

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Items: 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3293915	NM_001270875.3(MEAF6):c.25C>T (p.Pro9Ser)	LOC129930155, MEAF6 (P9S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3124779	NM_001270875.3(MEAF6):c.5C>T (p.Ala2Val)	LOC129930155, MEAF6 (A2V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2467374	NM_001270875.3(MEAF6):c.7A>G (p.Met3Val)	LOC129930155, MEAF6 (M3V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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