"PreventionGenetics, part of Exact Sciences"[submitter] AND "UBIAD1"[g - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 291825	NM_013319.3(UBIAD1):c.452A>G (p.Tyr151Cys)	UBIAD1 (Y151C)	Single nucleotide variant (missense variant)	UBIAD1-related disorder +2 more	GBenign
Select item 2636339	NM_013319.3(UBIAD1):c.991C>T (p.Pro331Ser)	UBIAD1 (P331S)	Single nucleotide variant (missense variant +1 more)	UBIAD1-related disorder	GUncertain significance
Select item 3030278	NM_001330349.2(UBIAD1):c.*7G>A	UBIAD1	Single nucleotide variant (3 prime UTR variant)	UBIAD1-related disorder	GLikely benign

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ClinVar