ClinVar Miner

Submissions for variant NM_020061.6(OPN1LW):c.511G>A (p.Val171Met)

dbSNP: rs5986963
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001788853 SCV002029307 benign Cone monochromatism 2021-09-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004714326 SCV005275071 benign not provided criteria provided, single submitter not provided

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