"PreventionGenetics, part of Exact Sciences"[submitter] AND "DMBX1"[ge - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3061007	NM_172225.2(DMBX1):c.444C>T (p.Ala148=)	DMBX1	Single nucleotide variant (synonymous variant)	DMBX1-related condition	GBenign
Select item 3052275	NM_172225.2(DMBX1):c.555G>A (p.Glu185=)	DMBX1	Single nucleotide variant (synonymous variant)	DMBX1-related condition	GLikely benign
Select item 3037813	NM_172225.2(DMBX1):c.598G>C (p.Ala200Pro)	DMBX1 (A200P +1 more)	Single nucleotide variant (missense variant)	DMBX1-related condition	GBenign
Select item 3034832	NM_172225.2(DMBX1):c.837G>A (p.Ser279=)	DMBX1	Single nucleotide variant (synonymous variant)	DMBX1-related condition	GLikely benign
Select item 3049412	NM_172225.2(DMBX1):c.854G>C (p.Gly285Ala)	DMBX1 (G285A +1 more)	Single nucleotide variant (missense variant)	DMBX1-related condition	GLikely benign
Select item 3048870	NM_172225.2(DMBX1):c.1003C>T (p.Leu335=)	DMBX1	Single nucleotide variant (synonymous variant)	DMBX1-related condition	GLikely benign
Select item 3054840	NM_172225.2(DMBX1):c.1007C>G (p.Pro336Arg)	DMBX1 (P336R +1 more)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity

ClinVar