ClinVar Miner

Submissions for variant NM_017637.6(BNC2):c.2920A>G (p.Ile974Val)

gnomAD frequency: 0.00945  dbSNP: rs35005898
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000948355 SCV001094559 benign not provided 2024-01-26 criteria provided, single submitter clinical testing
Centre for molecular medicine, Karolinska Institutet RCV000190268 SCV000143809 not provided Hypotension no assertion provided not provided

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