ClinVar Miner

Submissions for variant NM_001034853.2(RPGR):c.980T>G (p.Leu327Ter)

dbSNP: rs62640594
Minimum review status: Collection method:
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ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV000085139 SCV001249287 pathogenic not provided 2016-11-01 criteria provided, single submitter clinical testing
PreventionGenetics, part of Exact Sciences RCV000085139 SCV002759584 likely pathogenic not provided 2021-06-15 criteria provided, single submitter clinical testing
Retina International RCV000085139 SCV000117276 not provided not provided no assertion provided not provided

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