ClinVar Miner

Submissions for variant NM_016343.4(CENPF):c.9318C>G (p.Asn3106Lys)

dbSNP: rs7289
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001578978 SCV001806356 benign Stromme syndrome 2021-07-22 criteria provided, single submitter clinical testing
GeneDx RCV001707911 SCV001936044 benign not provided 2018-07-20 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 29765066)
Invitae RCV001707911 SCV002442602 benign not provided 2024-01-29 criteria provided, single submitter clinical testing

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