ClinVar Miner

Submissions for variant NM_004183.4(BEST1):c.933C>T (p.Val311=)

gnomAD frequency: 0.00003  dbSNP: rs281865278
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
Invitae RCV000086204 SCV003519313 likely benign not provided 2022-03-18 criteria provided, single submitter clinical testing
Retina International RCV000086204 SCV000118348 not provided not provided no assertion provided not provided

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