"Fulgent Genetics, Fulgent Genetics"[submitter] AND "DST"[gene] - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 795677	NM_001374736.1(DST):c.17923-10A>G	DST	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign
Select item 795666	NM_001374736.1(DST):c.15584G>A (p.Cys5195Tyr)	DST (C2898Y +6 more)	Single nucleotide variant (missense variant)	not provided +2 more	GBenign/Likely benign
Select item 798645	NM_001374736.1(DST):c.14461A>C (p.Asn4821His)	DST (N4610H +6 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GBenign/Likely benign
Select item 1338910	NM_001374736.1(DST):c.3495-17T>C	DST	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign

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