"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC126861 - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2039651	NM_001387274.1(DCDC1):c.754+9G>T	DCDC1, LOC126861175	Single nucleotide variant (intron variant)	DCDC1-related condition +1 more	GLikely benign
Select item 3040658	NM_001387274.1(DCDC1):c.616C>T (p.Leu206=)	DCDC1, LOC126861175	Single nucleotide variant (synonymous variant +1 more)	DCDC1-related condition	GLikely benign
Select item 1951466	NM_001387274.1(DCDC1):c.534T>G (p.Ala178=)	LOC126861175, DCDC1	Single nucleotide variant (synonymous variant +1 more)	DCDC1-related condition +1 more	GBenign

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ClinVar