ClinVar Miner

Submissions for variant NM_000255.4(MMUT):c.1677-20A>C

dbSNP: rs2127415238
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 RCV001492526 SCV001697138 likely benign not provided 2022-06-17 criteria provided, single submitter clinical testing

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