ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.7063A>C (p.Thr2355Pro)

dbSNP: rs2092400099
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Biochemical Molecular Genetic Laboratory, King Abdulaziz Medical City RCV001283798 SCV001469186 uncertain significance Polycystic kidney disease, adult type 2020-09-10 no assertion criteria provided clinical testing

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