ClinVar Miner

Submissions for variant NM_000929.3(PLA2G5):c.185G>A (p.Trp62Ter)

dbSNP: rs746408116
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000023077 SCV000044368 affects Familial benign flecked retina 2011-12-09 no assertion criteria provided literature only

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