"DCBLD2-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3060115	NM_080927.4(DCBLD2):c.2014A>G (p.Ile672Val)	DCBLD2 (I672V)	Single nucleotide variant (missense variant)	DCBLD2-related condition	GLikely benign
Select item 3038512	NM_080927.4(DCBLD2):c.1162G>A (p.Asp388Asn)	DCBLD2 (D388N)	Single nucleotide variant (missense variant)	DCBLD2-related condition	GLikely benign