List of variants in gene LYRM7 reported as likely 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: 3

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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.214C>G (p.Gln72Glu)	rs869025604
NM_181705.4(LYRM7):c.309del (p.Lys103fs)

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