ClinVar Miner

Submissions for variant NM_024513.4(FYCO1):c.3438-29C>T

gnomAD frequency: 0.45750  dbSNP: rs1532071
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001537006 SCV001753829 benign not provided 2018-07-21 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001702917 SCV001933676 benign Cataract 18 2021-08-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001537006 SCV005241700 benign not provided criteria provided, single submitter not provided

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