List of variants in gene RMRP reported as pathogenic by Victorian Clinical Genetics Services, Murdoch Childrens Research Institute

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
NR_003051.4(RMRP):n.240C>T	rs749667892	0.00016
NR_003051.3(RMRP):n.-5_-4insAACTACTCTGTGAAGCTGA	rs1408633343
NR_003051.4(RMRP):n.94dup	rs2131808768

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