List of variants in gene combination MIR6753, TCIRG1 reported as likely pathogenic for bone disorder

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_006019.4(TCIRG1):c.1021-1G>T	rs1590807544	0.00001
NM_006019.4(TCIRG1):c.723C>A (p.Cys241Ter)	rs2495623626

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