CN239242[trait identifier] AND "Illumina Laboratory Services, Illumina - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 313337	NM_001202.6(BMP4):c.*150del	BMP4	Deletion (3 prime UTR variant)	not provided +4 more	GUncertain significance
Select item 313344	NM_001202.6(BMP4):c.146_148dup	BMP4	Duplication (3 prime UTR variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 313343	NM_001202.6(BMP4):c.148_149insAG	BMP4	Insertion (3 prime UTR variant)	Cleft Lip +/- Cleft Palate, Autosomal Dominant +3 more	GUncertain significance
Select item 313342	NM_001202.6(BMP4):c.148_149insAAT	BMP4	Insertion (3 prime UTR variant)	Syndromic Microphthalmia, Dominant +4 more	GConflicting classifications of pathogenicity
Select item 313341	NM_001202.6(BMP4):c.148_149insT	BMP4	Insertion (3 prime UTR variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 313340	NM_001202.6(BMP4):c.145_149del	BMP4	Deletion (3 prime UTR variant)	Syndromic Microphthalmia, Dominant +3 more	GUncertain significance
Select item 313339	NM_001202.6(BMP4):c.148_149insAT	BMP4	Insertion (3 prime UTR variant)	not provided +4 more	GConflicting classifications of pathogenicity
Select item 313338	NM_001202.6(BMP4):c.148_149del	BMP4	Deletion (3 prime UTR variant)	Syndromic Microphthalmia, Dominant +4 more	GConflicting classifications of pathogenicity

ClinVar