C4304670[trait identifier] AND "GeneReviews"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 626332	NM_182978.4(GNAL):c.505-5T>C	GNAL	Single nucleotide variant (intron variant)	Dystonic disorder	GUncertain significance
Select item 626333	NM_182978.4(GNAL):c.964C>T (p.Arg322Ter)	GNAL (R245* +2 more)	Single nucleotide variant (nonsense)	not provided	GPathogenic
Select item 626331	NM_182978.4(GNAL):c.1163-7T>G	GNAL	Single nucleotide variant (intron variant)	not provided +1 more	GBenign

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