List of variants in gene RMND1 reported as likely benign for Combined oxidative phosphorylation defect type 11

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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: 7

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HGVS	dbSNP	gnomAD frequency
NM_017909.4(RMND1):c.1209T>C (p.Asn403=)	rs75177593	0.00108
NM_017909.4(RMND1):c.1167G>A (p.Thr389=)	rs116201484	0.00071
NM_017909.4(RMND1):c.690-20C>G	rs770275231	0.00011
NM_017909.4(RMND1):c.614-18G>A	rs764159292	0.00009
NM_017909.4(RMND1):c.1077A>G (p.Leu359=)	rs766598526	0.00004
NM_017909.4(RMND1):c.201C>A (p.Ile67=)	rs182333944	0.00001
NM_017909.4(RMND1):c.501C>T (p.Asn167=)	rs374790732	0.00001

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