"GeneDx"[submitter] AND "MIR3655"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59672	GRCh38/hg38 5q21.3-33.2(chr5:106619588-156124387)x1	ABLIM3, ACSL6 +1672 more	Copy number loss	See cases	GPathogenic
Select item 1205148	NC_000005.10:g.140647863C>T	IK, MIR3655 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 1190646	NC_000005.10:g.140647898A>T	IK, MIR3655 +1 more	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign

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