C3553247[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1028989	NM_006015.6(ARID1A):c.1712C>T (p.Ser571Leu)	ARID1A (S571L)	Single nucleotide variant (missense variant)	Intellectual disability, autosomal dominant 14 +1 more	GUncertain significance
Select item 434319	NM_006015.6(ARID1A):c.1803+9T>C	ARID1A	Single nucleotide variant (intron variant)	not specified +2 more	GLikely benign
Select item 434322	NM_006015.6(ARID1A):c.3408G>A (p.Ala1136=)	ARID1A, LOC126805670	Single nucleotide variant (synonymous variant)	not specified +3 more	GConflicting classifications of pathogenicity
Select item 434342	NM_006015.6(ARID1A):c.3978GCA[10] (p.Gln1333_Gln1334dup)	ARID1A	Microsatellite (inframe_insertion)	not specified +2 more	GLikely benign
Select item 210262	NM_006015.6(ARID1A):c.6586C>T (p.Leu2196=)	ARID1A	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 259583	NM_004924.6(ACTN4):c.929G>A (p.Arg310Gln)	ACTN4 (R310Q)	Single nucleotide variant (missense variant)	not provided +4 more	GBenign/Likely benign

ClinVar