List of variants in gene BMPR1B reported as pathogenic for bone disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NC_000004.11:g.(?_96025576)_(96036958_?)del
NM_001203.3(BMPR1B):c.1111C>T (p.Arg371Ter)
NM_001203.3(BMPR1B):c.1456C>T (p.Arg486Trp)	rs121434418
NM_001203.3(BMPR1B):c.157T>C (p.Cys53Arg)	rs863225041
NM_001203.3(BMPR1B):c.361_368del (p.Gly121fs)	rs863223287
NM_001203.3(BMPR1B):c.402_405del (p.Cys135fs)	rs1560671891
NM_001203.3(BMPR1B):c.640C>A (p.Arg214Ser)	rs1553941890
NM_001203.3(BMPR1B):c.657G>A (p.Trp219Ter)	rs863225042
NM_001203.3(BMPR1B):c.91C>T (p.Arg31Cys)	rs745854387

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