Related gene-specific medical variations for Gene (Select 729911) - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3011947	NR_029705.1(MIR184):n.55G>A	ANKRD34C-AS1, MIR184	Single nucleotide variant (non-coding transcript variant)	not provided	GLikely benign
Select item 1606846	NR_029705.1(MIR184):n.39G>T	ANKRD34C-AS1, MIR184	Single nucleotide variant (non-coding transcript variant)	not provided	GBenign
Select item 1065584	NR_029705.1(MIR184):n.52T>C	ANKRD34C-AS1, MIR184	Single nucleotide variant (non-coding transcript variant)	MIR184-related condition	GUncertain significance
Select item 31007	NR_029705.1(MIR184):n.57C>T	ANKRD34C-AS1, MIR184	Single nucleotide variant (non-coding transcript variant)	EDICT syndrome	GPathogenic

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