Related gene-specific medical variations for Gene (Select 126860943) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3055153	NM_032199.3(ARID5B):c.771A>G (p.Pro257=)	ARID5B, LOC126860943	Single nucleotide variant (synonymous variant)	ARID5B-related condition	GLikely benign
Select item 2462014	NM_032199.3(ARID5B):c.821A>G (p.Asn274Ser)	ARID5B, LOC126860943 (N274S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance