"PreventionGenetics, part of Exact Sciences"[submitter] AND "B3GNT2"[g - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3057724	NM_006577.6(B3GNT2):c.73A>G (p.Met25Val)	B3GNT2 (M25V)	Single nucleotide variant (missense variant)	B3GNT2-related condition	GLikely benign
Select item 3053280	NM_006577.6(B3GNT2):c.243G>C (p.Thr81=)	B3GNT2	Single nucleotide variant (synonymous variant)	B3GNT2-related condition	GLikely benign
Select item 709364	NM_006577.6(B3GNT2):c.309G>A (p.Thr103=)	B3GNT2	Single nucleotide variant (synonymous variant)	B3GNT2-related condition +1 more	GBenign
Select item 3057328	NM_006577.6(B3GNT2):c.1035C>T (p.Leu345=)	B3GNT2	Single nucleotide variant (synonymous variant)	B3GNT2-related condition	GLikely benign

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