List of variants in gene BMPR1B reported as likely benign by Illumina Laboratory Services, Illumina

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: 9

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HGVS	dbSNP	gnomAD frequency
NM_001203.3(BMPR1B):c.*9G>C	rs112333283	0.00314
NM_001203.3(BMPR1B):c.*413G>A	rs188703962	0.00198
NM_001203.3(BMPR1B):c.*2433A>G	rs139936115	0.00143
NM_001203.3(BMPR1B):c.*3101A>G	rs556715070	0.00100
NM_001203.3(BMPR1B):c.*1013C>T	rs191551226	0.00020
NM_001203.3(BMPR1B):c.150C>T (p.Asp50=)	rs147320212	0.00009
NM_001203.3(BMPR1B):c.-18+1G>T	rs761522559	0.00006
NM_001203.3(BMPR1B):c.395T>G (p.Val132Gly)	rs150002205	0.00004
NM_001203.3(BMPR1B):c.762G>T (p.Arg254Ser)	rs200198618	0.00001

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