ClinVar Miner

Submissions for variant NM_201548.5(CERKL):c.896-18T>C

dbSNP: rs13003064
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001543215 SCV001761731 benign Retinitis pigmentosa 26 2021-07-10 criteria provided, single submitter clinical testing

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