List of variants in gene TOP1MT reported as likely benign by Breakthrough Genomics, Breakthrough Genomics

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_052963.3(TOP1MT):c.1754G>A (p.Arg585Gln)	rs147154528	0.00116
NM_052963.3(TOP1MT):c.1030C>T (p.Arg344Cys)	rs72701720	0.00106
NM_052963.3(TOP1MT):c.133G>A (p.Glu45Lys)	rs150542670	0.00089
NM_052963.3(TOP1MT):c.147C>T (p.Asp49=)	rs147991386	0.00081

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