ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.12403dup (p.Arg4135fs)

dbSNP: rs2091435565
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
CeGaT Center for Human Genetics Tuebingen RCV001091870 SCV001248129 pathogenic not provided 2019-11-01 criteria provided, single submitter clinical testing

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