C2748515[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 779934	NM_001015880.2(PAPSS2):c.267C>T (p.Leu89=)	PAPSS2	Single nucleotide variant (synonymous variant)	Spondyloepimetaphyseal dysplasia, PAPSS2 type	GBenign/Likely benign
Select item 1636427	NM_001015880.2(PAPSS2):c.381+7_381+24dup	PAPSS2	Duplication (intron variant)	Spondyloepimetaphyseal dysplasia, PAPSS2 type	GLikely benign