List of variants in gene RMRP reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 4

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HGVS	dbSNP	gnomAD frequency
NR_003051.4(RMRP):n.129G>C	rs74810894	0.00319
NR_003051.4(RMRP):n.55C>T	rs193117694	0.00303
NR_003051.4(RMRP):n.141A>G	rs578091934	0.00042
NR_003051.4(RMRP):n.47T>A	rs529328233

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