ClinVar Miner

Submissions for variant NM_138694.4(PKHD1):c.1119-102_1119-100del

dbSNP: rs149924869
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001615650 SCV001835782 benign not provided 2018-07-09 criteria provided, single submitter clinical testing

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