List of variants in gene RMRP reported as uncertain significance by 3billion

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.232C>T	rs762145032	0.00001
NR_003051.3(RMRP):n.-24_-1dup	rs1823632816
NR_003051.3(RMRP):n.5_6insTACTCTGTGAAGCTGAGGACGTGGTTC	rs1554651349

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