"GeneDx"[submitter] AND "KCNJ18"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59297	GRCh38/hg38 17p11.2(chr17:20879426-22533437)x3	CCDC144NL-AS1, DHRS7B +41 more	Copy number gain	See cases	GUncertain significance
Select item 1295652	NC_000017.11:g.21416665A>G	KCNJ12, KCNJ18	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1235905	NM_001194958.2(KCNJ18):c.87C>T (p.Asn29=)	KCNJ18	Single nucleotide variant (synonymous variant)	not provided	GBenign

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