List of variants in gene RMRP reported as pathogenic by GeneDx

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: 5

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HGVS	dbSNP	gnomAD frequency
NR_003051.4(RMRP):n.6C>T	rs772443941	0.00016
NC_000009.12:g.35658031_35658037dup	rs1554651506	0.00005
NC_000009.12:g.35657872C>T	rs753874439
NR_003051.4(RMRP):n.-18_-2dup	rs727502778
NR_003051.4(RMRP):n.216A>C	rs886041234

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