Variants in gene SLC25A13 with conflicting interpretations "benign" and "likely benign"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 5

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HGVS	dbSNP	gnomAD frequency
NM_014251.3(SLC25A13):c.615+36T>C	rs56773234	0.01220
NM_014251.3(SLC25A13):c.1680C>T (p.Ser560=)	rs150082469	0.00244
NM_014251.3(SLC25A13):c.1452+19del	rs749506606
NM_014251.3(SLC25A13):c.848+8G>T	rs761126981
NM_014251.3(SLC25A13):c.848+9G>T	rs201395793

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