ClinVar Miner

Submissions for variant NM_173551.5(ANKS6):c.2327-19dup

dbSNP: rs575021016
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002124982 SCV002403100 benign Nephronophthisis 16 2024-06-15 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002124982 SCV002802313 likely benign Nephronophthisis 16 2021-08-25 criteria provided, single submitter clinical testing

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