List of variants in gene RMRP reported as pathogenic by CeGaT Center for Human Genetics Tuebingen

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
NR_003051.4(RMRP):n.6C>T	rs772443941	0.00016
NC_000009.12:g.35657921C>T	rs915919453	0.00001
NC_000009.12:g.35657756C>G	rs727502774
NR_003051.4(RMRP):n.97_98dup	rs1340624774

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