"Fulgent Genetics, Fulgent Genetics"[submitter] AND "CLCC1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 163641	NM_013296.5(GPSM2):c.1816-8A>G	CLCC1, GPSM2	Single nucleotide variant (3 prime UTR variant +2 more)	Chudley-McCullough syndrome +2 more	GBenign/Likely benign
Select item 211100	NM_013296.5(GPSM2):c.1909C>T (p.Arg637Trp)	CLCC1, GPSM2 (R637W)	Single nucleotide variant (3 prime UTR variant +2 more)	Chudley-McCullough syndrome +2 more	GConflicting classifications of pathogenicity