"Fulgent Genetics, Fulgent Genetics"[submitter] AND "DTNBP1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1615910	NM_032122.5(DTNBP1):c.512-16T>C	DTNBP1	Single nucleotide variant (intron variant)	Hermansky-Pudlak syndrome 7 +1 more	GLikely benign
Select item 1575214	NM_032122.5(DTNBP1):c.355+10A>G	DTNBP1	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 98379	NM_032122.5(DTNBP1):c.324C>T (p.Ile108=)	DTNBP1	Single nucleotide variant (synonymous variant +1 more)	Hermansky-Pudlak syndrome 7 +1 more	GLikely benign

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