Variants in gene BMPR1A with conflicting interpretations "uncertain significance" and "uncertain significance"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 3

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HGVS	dbSNP	gnomAD frequency
NM_004329.3(BMPR1A):c.1243G>A (p.Glu415Lys)	rs140592056	0.00051
NM_004329.3(BMPR1A):c.1433G>A (p.Arg478His)	rs113849804	0.00025
NM_004329.3(BMPR1A):c.1596C>G (p.Ile532Met)	rs201345248	0.00003

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