ClinVar Miner

Submissions for variant NM_153485.3(NUP155):c.201G>A (p.Leu67=)

gnomAD frequency: 0.96886  dbSNP: rs217852
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001538213 SCV001755829 benign not provided 2021-05-04 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001788587 SCV002029734 benign Atrial fibrillation, familial, 15 2021-09-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001538213 SCV005298054 benign not provided criteria provided, single submitter not provided

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