"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 1672570	NM_001286577.2(C2CD3):c.5769G>A (p.Gln1923=)	C2CD3, LOC126861262	Single nucleotide variant (synonymous variant)	C2CD3-related condition +1 more	GLikely benign
Select item 2790430	NM_001286577.2(C2CD3):c.5748A>G (p.Gln1916=)	C2CD3, LOC126861262	Single nucleotide variant (synonymous variant)	C2CD3-related condition +1 more	GLikely benign