"Genome-Nilou Lab"[submitter] AND "LOC129997524"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 624273	NM_001374828.1(ARID1B):c.417C>G (p.Gly139=)	ARID1B, LOC115308161 +1 more	Single nucleotide variant (synonymous variant)	Coffin-Siris syndrome 1 +2 more	GLikely benign
Select item 210272	NM_001374828.1(ARID1B):c.446A>G (p.Asn149Ser)	ARID1B, LOC115308161 +1 more (N66S +1 more)	Single nucleotide variant (missense variant)	not specified +3 more	GConflicting classifications of pathogenicity