"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "LOC1299 - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 534541	NC_000002.11:g.(?_233390906)_(233410446_?)dup	CHRND, CHRNG +2 more	Duplication	Lethal multiple pterygium syndrome	GUncertain significance
Select item 2996857	NM_005199.5(CHRNG):c.492C>T (p.Cys164=)	CHRNG, LOC129935864	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2856780	NM_005199.5(CHRNG):c.506+12T>C	CHRNG, LOC129935864	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2981211	NM_005199.5(CHRNG):c.506+14T>C	CHRNG, LOC129935864	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2716193	NM_005199.5(CHRNG):c.506+15T>G	CHRNG, LOC129935864	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2715704	NM_005199.5(CHRNG):c.506+20A>T	CHRNG, LOC129935864	Single nucleotide variant (intron variant)	not provided	GLikely benign

ClinVar