ClinVar Miner

Submissions for variant NM_138694.4(PKHD1):c.7351-21dup

dbSNP: rs768522482
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Counsyl RCV000668540 SCV000793161 likely benign Autosomal recessive polycystic kidney disease 2017-08-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000668540 SCV003490679 benign Autosomal recessive polycystic kidney disease 2023-11-06 criteria provided, single submitter clinical testing

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