"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC126862 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 728173	NM_001365088.1(SLC12A6):c.2613C>T (p.Arg871=)	LOC126862097, SLC12A6	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 315608	NM_001365088.1(SLC12A6):c.2565G>A (p.Thr855=)	SLC12A6, LOC126862097	Single nucleotide variant (synonymous variant)	SLC12A6-related disorder +3 more	GConflicting classifications of pathogenicity