ClinVar Miner

Variants with conflicting interpretations "uncertain significance" from Medical & Molecular Genetics Group,University of Lincoln and "benign" from any submitter

Minimum review status of the submission from Medical & Molecular Genetics Group,University of Lincoln: Collection method of the submission from Medical & Molecular Genetics Group,University of Lincoln:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 1
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HGVS dbSNP
NM_001204.7(BMPR2):c.1766A>G (p.Tyr589Cys) rs199915496

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