List of variants in gene RMRP reported as likely benign for not specified

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: 10

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HGVS	dbSNP	gnomAD frequency
NR_003051.4(RMRP):n.129G>C	rs74810894	0.00319
NR_003051.3(RMRP):n.-3C>T	rs138660393	0.00185
NR_003051.3(RMRP):n.-7A>G	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.35658122G>A	rs1554651647
NR_003051.3(RMRP):n.-4A>G	rs555890962
NR_003051.3(RMRP):n.-56C>G	rs531089786
NR_003051.3(RMRP):n.-5G>C	rs7024732
NR_003051.3(RMRP):n.-9T>G	rs12552387

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