"Ambry Genetics"[submitter] AND "LOC107105350"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2374769	NM_014212.4(HOXC11):c.569C>G (p.Ala190Gly)	HOTAIR, HOXC11 +1 more (A190G)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2228996	NM_014212.4(HOXC11):c.574C>G (p.Arg192Gly)	HOTAIR, HOXC11 +1 more (R192G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance