"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "CHRM1"[ - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 741059	NM_000738.3(CHRM1):c.1137A>C (p.Thr379=)	CHRM1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 715306	NM_000738.3(CHRM1):c.843C>T (p.Asp281=)	CHRM1	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 746110	NM_000738.3(CHRM1):c.732T>A (p.Ser244=)	CHRM1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 708735	NM_000738.3(CHRM1):c.690G>A (p.Thr230=)	CHRM1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2163220	NM_000738.3(CHRM1):c.238A>C (p.Asn80His)	CHRM1 (N80H)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 741447	NM_000738.3(CHRM1):c.42C>T (p.Thr14=)	CHRM1	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2425028	NC_000011.9:g.(?_58916346)_(64972349_?)dup	AHNAK, ARL2 +182 more	Duplication	Leukocyte adhesion deficiency 3	GUncertain significance

ClinVar