ClinVar Miner

Submissions for variant NM_138694.4(PKHD1):c.11506+32dup

dbSNP: rs376358912
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001715925 SCV001946627 benign not provided 2019-08-21 criteria provided, single submitter clinical testing
Natera, Inc. RCV001827588 SCV002075479 benign Autosomal recessive polycystic kidney disease 2017-05-15 no assertion criteria provided clinical testing

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