List of variants in gene RMND1 reported as benign for combined oxidative phosphorylation deficiency

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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
NM_017909.4(RMND1):c.1002+47T>G	rs6912830	0.54650
NM_017909.4(RMND1):c.689+17A>G	rs6904364	0.42255
NM_017909.4(RMND1):c.125G>T (p.Ser42Ile)	rs11550103	0.09721
NM_017909.4(RMND1):c.783C>T (p.Ile261=)	rs17081207	0.00841

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