ClinVar Miner

Submissions for variant NM_025074.7(FRAS1):c.2313G>A (p.Pro771=)

dbSNP: rs396790
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 RCV000911067 SCV001056120 likely benign not provided 2024-01-25 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002505337 SCV002806136 likely benign Fraser syndrome 1 2022-03-02 criteria provided, single submitter clinical testing

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