List of variants in gene RMRP reported as likely benign 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: 9

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HGVS	dbSNP	gnomAD frequency
NC_000009.12:g.35658025T>C	rs111909453	0.00057
NR_003051.4(RMRP):n.141A>G	rs578091934	0.00042
NR_003051.4(RMRP):n.86T>G	rs991322091	0.00001
NC_000009.12:g.35658022T>C	rs555890962
NC_000009.12:g.35658023C>G	rs7024732
NC_000009.12:g.35658027A>C	rs12552387
NC_000009.12:g.35658074G>C	rs531089786
NC_000009.12:g.35658122G>A	rs1554651647
NR_003051.4(RMRP):n.1T>C	rs188190570

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