"GeneDx"[submitter] AND "MIR6810"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59159	GRCh38/hg38 2q32.2-37.3(chr2:190310736-241892770)x3	LOC129935726, LOC129935727 +1665 more	Copy number gain	See cases	GPathogenic
Select item 1250259	NM_015488.5(PNKD):c.618-59A>G	CATIP-AS2, MIR6810 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign
Select item 1219889	NM_015488.5(PNKD):c.618-58C>T	CATIP-AS2, MIR6810 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign

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