ClinVar Miner

Submissions for variant NM_138694.4(PKHD1):c.6866-4_6866-2del

dbSNP: rs748114217
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000668657 SCV000793291 uncertain significance Autosomal recessive polycystic kidney disease 2017-08-09 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002485546 SCV002784268 uncertain significance Polycystic kidney disease 4 2021-09-07 criteria provided, single submitter clinical testing

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