ClinVar Miner

Submissions for variant NM_006915.3(RP2):c.768+13A>G

gnomAD frequency: 0.00001  dbSNP: rs1284693367
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
Labcorp Genetics (formerly Invitae), Labcorp RCV002126011 SCV002452264 likely benign not provided 2024-12-04 criteria provided, single submitter clinical testing

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