"Invitae"[submitter] AND "LOC130009581"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1027899	NM_181503.3(EXOSC8):c.13T>C (p.Phe5Leu)	LOC130009581, EXOSC8 (F5L)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 1921827	NM_181503.3(EXOSC8):c.17+7G>A	EXOSC8, LOC130009581	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 712129	NM_181503.3(EXOSC8):c.17+8T>C	EXOSC8, LOC130009581	Single nucleotide variant (intron variant)	not provided	GLikely benign

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