Variants in gene SLC13A5 with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) 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: 10

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HGVS	dbSNP	gnomAD frequency
NM_177550.5(SLC13A5):c.655G>A (p.Gly219Arg)	rs144332569	0.00009
NM_177550.5(SLC13A5):c.680C>T (p.Thr227Met)	rs587777577	0.00004
NM_177550.5(SLC13A5):c.997C>T (p.Arg333Ter)	rs773770609	0.00004
NM_177550.5(SLC13A5):c.1022G>A (p.Trp341Ter)	rs150203483	0.00001
NM_177550.5(SLC13A5):c.1280C>T (p.Ser427Leu)	rs548065551	0.00001
NM_177550.5(SLC13A5):c.425C>T (p.Thr142Met)	rs761917087	0.00001
NM_177550.5(SLC13A5):c.1276-1G>A	rs1597657030
NM_177550.5(SLC13A5):c.1463T>C (p.Leu488Pro)	rs587777578
NM_177550.5(SLC13A5):c.1475T>C (p.Leu492Pro)	rs1057519449
NM_177550.5(SLC13A5):c.1511del (p.Leu504fs)	rs1211773372

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