List of variants in gene RMRP reported as likely pathogenic for not provided

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.81G>A	rs756128568	0.00004
NR_003051.4(RMRP):n.16G>T	rs902313238	0.00002
NC_000009.12:g.35657873G>A	rs757576534
NC_000009.12:g.35658022_35658032dup	rs1554651425
NC_000009.12:g.35658023_35658038dup	rs1823637651
NC_000009.12:g.35658032_35658045dup	rs1554651499
NR_003051.3(RMRP):n.-7_1dup8	rs752934195
NR_003051.3(RMRP):r.-25_-7dupTACTACTCTGTGAAGCTGA	rs1554651455
NR_003051.4(RMRP):n.149C>T	rs1085307765
NR_003051.4(RMRP):n.52C>T	rs1064793373

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