"Fulgent Genetics, Fulgent Genetics"[submitter] AND "BMP4"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1006001	NM_001202.6(BMP4):c.935C>T (p.Ser312Leu)	BMP4 (S249L +2 more)	Single nucleotide variant (missense variant)	Microphthalmia with brain and digit anomalies +1 more	GUncertain significance
Select item 1691786	NM_001202.6(BMP4):c.863G>A (p.Arg288Gln)	BMP4 (R225Q +2 more)	Single nucleotide variant	Microphthalmia with brain and digit anomalies +3 more	GConflicting classifications of pathogenicity
Select item 1022631	NM_001202.6(BMP4):c.857G>A (p.Arg286Gln)	BMP4 (R223Q +2 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GUncertain significance
Select item 1371084	NM_001202.6(BMP4):c.668G>A (p.Arg223His)	BMP4 (R270H +2 more)	Single nucleotide variant (missense variant)	Microphthalmia with brain and digit anomalies +1 more	GUncertain significance
Select item 434517	NM_001202.6(BMP4):c.252G>A (p.Arg84=)	BMP4	Single nucleotide variant (synonymous variant)	not specified +2 more	GLikely benign
Select item 313353	NM_001202.6(BMP4):c.224A>G (p.Lys75Arg)	BMP4 (K75R +2 more)	Single nucleotide variant (missense variant)	Microphthalmia with brain and digit anomalies +4 more	GUncertain significance
Select item 721286	NM_001202.6(BMP4):c.93G>C (p.Gly31=)	BMP4	Single nucleotide variant (synonymous variant +1 more)	Orofacial cleft 11 +1 more	GLikely benign

ClinVar