ClinVar Miner

Submissions for variant NM_000297.4(PKD2):c.1587A>T (p.Thr529=)

dbSNP: rs375543446
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV000541429 SCV000658967 benign Autosomal dominant polycystic kidney disease 2024-01-29 criteria provided, single submitter clinical testing
GeneDx RCV002293458 SCV002586740 likely benign not provided 2022-04-24 criteria provided, single submitter clinical testing

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