List of variants in gene TCIRG1 reported as pathogenic for TCIRG1-related condition

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_006019.4(TCIRG1):c.1674-1G>A	rs139617644	0.00019
NM_006019.4(TCIRG1):c.1230del (p.Leu411fs)	rs2134454279
NM_006019.4(TCIRG1):c.692del (p.Lys231fs)

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