List of variants in gene BMP4 reported as uncertain significance for Orofacial cleft

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_001202.6(BMP4):c.148_149del	rs140085940	0.04744
NM_001202.6(BMP4):c.*251C>T	rs573118445	0.00021
NM_001202.6(BMP4):c.215A>G (p.Gln72Arg)	rs771047931	0.00001
NM_001202.6(BMP4):c.145_149del	rs886050539
NM_001202.6(BMP4):c.146_148dup	rs1555339771
NM_001202.6(BMP4):c.148_149insAAT	rs796563569
NM_001202.6(BMP4):c.148_149insAG	rs796563569
NM_001202.6(BMP4):c.148_149insAT	rs796563569
NM_001202.6(BMP4):c.148_149insT	rs796563569
NM_001202.6(BMP4):c.*149G>A	rs74495140
NM_001202.6(BMP4):c.*150del	rs878985651
NM_001202.6(BMP4):c.370+12C>T	rs368426865

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