"Invitae"[submitter] AND "MIR6752"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1585349	NM_003977.4(AIP):c.646-20C>G	AIP, MIR6752	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1429633	NM_003977.4(AIP):c.646-18C>T	AIP, MIR6752	Single nucleotide variant (intron variant +1 more)	not provided	GLikely benign
Select item 1581829	NM_003977.4(AIP):c.646-14C>T	AIP, MIR6752	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1566651	NM_003977.4(AIP):c.646-12C>T	AIP, MIR6752	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1652039	NM_003977.4(AIP):c.646-10A>T	MIR6752, AIP	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1643181	NM_003977.4(AIP):c.646-10A>G	AIP, MIR6752	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1930944	NM_003977.4(AIP):c.646-4C>T	AIP, MIR6752	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1362636	NM_003977.4(AIP):c.646-3C>T	AIP, MIR6752	Single nucleotide variant (intron variant +1 more)	not provided	GUncertain significance

ClinVar