Related gene-specific medical variations for Gene (Select 57146) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3083958	NM_001301771.2(LDAF1):c.-99+617T>A	DNAH3, LDAF1 (R27W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3083932	NM_001301771.2(LDAF1):c.-99+640G>C	DNAH3, LDAF1 (P19R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2209843	NM_001301771.2(LDAF1):c.-99+628C>A	DNAH3, LDAF1 (R23L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2206001	NM_001301771.2(LDAF1):c.-99+594T>A	DNAH3, LDAF1 (E34D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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