ClinVar Miner

Submissions for variant NM_000128.4(F11):c.1481-15_1481-14insCC

dbSNP: rs2477416165
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 RCV003564813 SCV004322919 likely benign not provided 2023-09-10 criteria provided, single submitter clinical testing

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