ClinVar Miner

Submissions for variant NM_002018.4(FLII):c.3772T>C (p.Phe1258Leu)

dbSNP: rs1567701499
Minimum review status: Collection method:
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Institute of Human Genetics, Polish Academy of Sciences RCV000785720 SCV000891426 uncertain significance High myopia 2018-12-17 no assertion criteria provided research

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