"GeneDx"[submitter] AND "LOC126806063"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58116	GRCh38/hg38 1q32.2-44(chr1:209646207-248931113)x3	OR2M4, OR2M5 +1351 more	Copy number gain	See cases	GPathogenic
Select item 511214	NM_000081.4(LYST):c.9926-12C>T	LOC126806063, LYST	Single nucleotide variant (intron variant)	not specified +1 more	GLikely benign
Select item 684363	NM_000081.4(LYST):c.9926-57A>G	LOC126806063, LYST	Single nucleotide variant (intron variant)	not specified +1 more	GBenign

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