ClinVar Miner

Submissions for variant NM_002336.3(LRP6):c.1426C>G (p.Leu476Val)

dbSNP: rs2136988022
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Gastroenterology and Hepatology, Radboud University Medical Center RCV001844910 SCV001877043 uncertain significance Autosomal dominant polycystic liver disease 2021-09-01 no assertion criteria provided research

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