ClinVar Miner

Submissions for variant NM_025074.7(FRAS1):c.10540+15G>A

gnomAD frequency: 0.00009  dbSNP: rs766110910
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
Labcorp Genetics (formerly Invitae), Labcorp RCV002125913 SCV002450413 likely benign not provided 2024-01-03 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494419 SCV002794871 likely benign Fraser syndrome 1 2021-07-30 criteria provided, single submitter clinical testing

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