"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "HS6ST2" - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 711149	NM_001394073.1(HS6ST2):c.975A>G (p.Ala325=)	HS6ST2	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 714969	NM_001394073.1(HS6ST2):c.321G>T (p.Leu107=)	HS6ST2	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 770313	NM_001394073.1(HS6ST2):c.152G>T (p.Arg51Leu)	HS6ST2 (R51L)	Single nucleotide variant (missense variant)	not provided	GBenign

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