"Labcorp Genetics (formerly Invitae), Labcorp"[submitter] AND "LOC1300 - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1601975	NM_003737.4(DCHS1):c.9201A>G (p.Ser3067=)	DCHS1, LOC130005209	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +1 more	GLikely benign
Select item 749231	NM_003737.4(DCHS1):c.9186C>T (p.Ala3062=)	DCHS1, LOC130005209	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3022590	NM_003737.4(DCHS1):c.9181G>A (p.Ala3061Thr)	DCHS1, LOC130005209 (A3061T)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 2874965	NM_003737.4(DCHS1):c.9173C>G (p.Ser3058Cys)	DCHS1, LOC130005209 (S3058C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1950202	NM_003737.4(DCHS1):c.9159G>T (p.Val3053=)	DCHS1, LOC130005209	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2054591	NM_003737.4(DCHS1):c.9155G>A (p.Arg3052His)	DCHS1, LOC130005209 (R3052H)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1379936	NM_003737.4(DCHS1):c.9154C>T (p.Arg3052Cys)	DCHS1, LOC130005209 (R3052C)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2779363	NM_003737.4(DCHS1):c.9150C>T (p.Phe3050=)	DCHS1, LOC130005209	Single nucleotide variant (synonymous variant)	not provided	GLikely benign

ClinVar