List of variants in gene LYRM7 reported as pathogenic for Mitochondrial complex III deficiency nuclear type 8

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_181705.4(LYRM7):c.2T>C (p.Met1Thr)	rs531275086	0.00002
NM_181705.4(LYRM7):c.190TTA[3] (p.Leu66dup)	rs869025603
NM_181705.4(LYRM7):c.214C>T (p.Gln72Ter)	rs869025604
NM_181705.4(LYRM7):c.244+5dup	rs869025602
NM_181705.4(LYRM7):c.37del (p.Thr13fs)	rs869025605
NM_181705.4(LYRM7):c.73G>A (p.Asp25Asn)	rs587777433

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