List of variants in gene RMRP reported as uncertain significance 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: 7

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HGVS	dbSNP	gnomAD frequency
NR_003051.4(RMRP):n.129G>C	rs74810894	0.00319
NR_003051.4(RMRP):n.125C>A	rs758130879	0.00022
NR_003051.4(RMRP):n.59_60insA	rs1053360711	0.00021
NR_003051.4(RMRP):n.113C>G	rs1479610947	0.00001
NR_003051.4(RMRP):n.86T>G	rs991322091	0.00001
NC_000009.12:g.35657873G>A	rs757576534
NR_003051.4(RMRP):n.81G>T	rs756128568

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