ClinVar Miner

Submissions for variant NM_015102.5(NPHP4):c.2688G>T (p.Arg896=)

gnomAD frequency: 0.00001  dbSNP: rs1421932012
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV003746560 SCV001012888 likely benign Nephronophthisis 2023-03-27 criteria provided, single submitter clinical testing

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