ClinVar Miner

Submissions for variant NM_001009944.3(PKD1):c.10220+2_10220+3del

dbSNP: rs1114167366
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, Cologne University RCV000490641 SCV000538205 pathogenic Polycystic kidney disease, adult type no assertion criteria provided clinical testing

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