List of variants in gene MTR reported as likely pathogenic for not provided

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_000254.3(MTR):c.1_2del (p.Met1fs)	rs1367402633	0.00001
NM_000254.3(MTR):c.2003del (p.Asn668fs)	rs1064796330
NM_000254.3(MTR):c.2432dup (p.Cys812fs)	rs1665274096
NM_000254.3(MTR):c.2595-2A>G	rs1558334603

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