ClinVar Miner

Submissions for variant NC_000002.12:g.(?_202467509)_(202467699_?)del

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001031309 SCV001194615 pathogenic Pulmonary hypertension, primary, 1 2019-12-16 criteria provided, single submitter clinical testing This variant is an in-frame deletion of the genomic region encompassing exon 3 of the BMPR2 gene. It preserves the integrity of the reading frame. This variant has been observed in individual(s) with pulmonary arterial hypertension (PMID: 28388887, 16728714, 21801371). This variant disrupts the p.Cys99 amino acid residue in BMPR2. Other variant(s) that disrupt this residue have been determined to be pathogenic (PMID: 19555857, 30578397, Invitae). This suggests that this residue is clinically significant, and that variants that disrupt this residue are likely to be disease-causing. For these reasons, this variant has been classified as Pathogenic.
Labcorp Genetics (formerly Invitae), Labcorp RCV001383551 SCV001582717 pathogenic Primary pulmonary hypertension 2020-10-18 criteria provided, single submitter clinical testing This variant is an in-frame deletion of the genomic region encompassing exon 3 of the BMPR2 gene. It preserves the integrity of the reading frame. This variant has been observed in individual(s) with pulmonary arterial hypertension (PMID: 28388887, 16728714, 21801371). This variant disrupts the p.Cys99 amino acid residue in BMPR2. Other variant(s) that disrupt this residue have been determined to be pathogenic (PMID: 19555857, 30578397, Invitae). This suggests that this residue is clinically significant, and that variants that disrupt this residue are likely to be disease-causing. For these reasons, this variant has been classified as Pathogenic.

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