"Invitae"[submitter] AND "MIR6753"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2918856	NM_006019.4(TCIRG1):c.1021-14G>A	MIR6753, TCIRG1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2148533	NM_006019.4(TCIRG1):c.1021-14G>T	MIR6753, TCIRG1	Single nucleotide variant (intron variant +1 more)	not provided	GLikely benign
Select item 2758589	NM_006019.4(TCIRG1):c.1021-11C>T	MIR6753, TCIRG1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2790166	NM_006019.4(TCIRG1):c.1021-5C>T	MIR6753, TCIRG1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2693622	NM_006019.4(TCIRG1):c.1021-2A>G	MIR6753, TCIRG1	Single nucleotide variant (splice acceptor variant +1 more)	not provided	GLikely pathogenic
Select item 2749238	NM_006019.4(TCIRG1):c.1021-1G>C	TCIRG1, MIR6753	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely pathogenic
Select item 1487056	NM_006019.4(TCIRG1):c.1021-1G>T	MIR6753, TCIRG1	Single nucleotide variant (non-coding transcript variant +1 more)	not provided +1 more	GLikely pathogenic

ClinVar