ClinVar Miner

Submissions for variant NC_000016.10:g.2092048_2092049dup

dbSNP: rs1596482597
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
Institute of Human Genetics Munich, Klinikum Rechts Der Isar, TU München RCV000995839 SCV001150213 pathogenic Polycystic kidney disease, adult type 2019-08-19 criteria provided, single submitter clinical testing

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