List of variants in gene RMRP reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 11

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HGVS	dbSNP	gnomAD frequency
NR_003051.4(RMRP):n.55C>T	rs193117694	0.00303
NC_000009.12:g.35658021G>A	rs138660393	0.00185
NC_000009.12:g.35658030T>G	rs372044910	0.00058
NC_000009.12:g.35658025T>C	rs111909453	0.00057
NR_003051.4(RMRP):n.141A>G	rs578091934	0.00042
NR_003051.4(RMRP):n.164C>T	rs550203343	0.00022
NC_000009.12:g.35658028G>A	rs572830134
NC_000009.12:g.35658042T>C	rs529852688
NC_000009.12:g.35658043A>G
NR_003051.4(RMRP):n.268G>C	rs535022008
NR_003051.4(RMRP):n.47T>A	rs529328233

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