ClinVar Miner

Submissions for variant NM_000554.6(CRX):c.100+2T>C

dbSNP: rs281865198
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
CeGaT Center for Human Genetics Tuebingen RCV000085986 SCV000892274 likely pathogenic not provided 2018-07-01 criteria provided, single submitter clinical testing
Retina International RCV000085986 SCV000118129 not provided not provided no assertion provided not provided

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