List of variants in gene RMRP reported as benign by Breakthrough Genomics, Breakthrough Genomics

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
NC_000009.12:g.35658065G>T	rs3829076	0.46029
NR_003051.4(RMRP):n.179C>T	rs7021642	0.17814
NC_000009.12:g.35657744A>G	rs71521283	0.17718
NR_003051.4(RMRP):n.158G>C	rs7021463	0.17549
NC_000009.12:g.35658023C>T	rs7024732
NC_000009.12:g.35658073T>C	rs12551232
NC_000009.12:g.35658075A>G	rs3829077

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