Related gene-specific medical variations for Gene (Select 100616397) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1687676	NM_001378414.1(HDAC4):c.2751-225C>A	HDAC4, MIR4440	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1278328	NM_001378414.1(HDAC4):c.2751-246A>G	HDAC4, MIR4440	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1268422	NM_001378414.1(HDAC4):c.2751-289A>C	HDAC4, MIR4440	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1232800	NM_001378414.1(HDAC4):c.2751-251C>T	HDAC4, MIR4440	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1229352	NM_001378414.1(HDAC4):c.2751-259C>A	HDAC4, MIR4440	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign

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