List of variants in gene RMND1 reported as pathogenic for Mitochondrial disease

Minimum submission review status:		Collection method:
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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: 9

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HGVS	dbSNP	gnomAD frequency
NM_017909.4(RMND1):c.713A>G (p.Asn238Ser)	rs144972972	0.00013
NM_017909.4(RMND1):c.565C>T (p.Gln189Ter)	rs886037772	0.00003
NM_017909.4(RMND1):c.1250G>A (p.Arg417Gln)	rs397515421	0.00002
NM_017909.4(RMND1):c.830+1G>A	rs773470671	0.00002
NM_017909.4(RMND1):c.1317+1G>T	rs886037773	0.00001
NM_017909.4(RMND1):c.1303C>T (p.Leu435Phe)	rs886037771
NM_017909.4(RMND1):c.1349G>C (p.Ter450Ser)	rs115079861
NM_017909.4(RMND1):c.533C>A (p.Thr178Lys)	rs370863743
NM_017909.4(RMND1):c.631G>A (p.Val211Met)	rs771894262

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