"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC102723 - ClinVar - NCBI

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Items: 3

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1099682	NM_022166.4(XYLT1):c.1905C>T (p.Tyr635=)	LOC102723692, XYLT1	Single nucleotide variant (synonymous variant)	XYLT1-related disorder +1 more	GLikely benign
Select item 732055	NM_022166.4(XYLT1):c.1716C>T (p.Cys572=)	LOC102723692, XYLT1	Single nucleotide variant (non-coding transcript variant +1 more)	XYLT1-related disorder +1 more	GLikely benign
Select item 788713	NM_022166.4(XYLT1):c.1626C>T (p.Cys542=)	LOC102723692, XYLT1	Single nucleotide variant (non-coding transcript variant +1 more)	XYLT1-related disorder +1 more	GBenign/Likely benign

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