List of variants in gene RMRP reported as 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: 7

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HGVS	dbSNP	gnomAD frequency
NR_003051.3(RMRP):n.-47C>A	rs3829076	0.46029
NR_003051.4(RMRP):n.179C>T	rs7021642	0.17814
NR_003051.4(RMRP):n.158G>C	rs7021463	0.17549
NR_003051.4(RMRP):n.177G>A	rs377566038	0.00039
NR_003051.3(RMRP):n.-20C>G	rs183974004
NR_003051.3(RMRP):n.-23C>G	rs188660894
NR_003051.4(RMRP):n.54dup	rs151011853

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