"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC129930 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3040409	NM_005540.3(INPP5B):c.532+215C>T	INPP5B, LOC129930172	Single nucleotide variant (synonymous variant +3 more)	INPP5B-related disorder	GBenign
Select item 3055357	NM_005540.3(INPP5B):c.532+213G>T	INPP5B, LOC129930172 (A5S)	Single nucleotide variant (missense variant +3 more)	INPP5B-related disorder	GBenign