ClinVar Miner

Submissions for variant NM_025074.7(FRAS1):c.10649-18T>C

gnomAD frequency: 0.00028  dbSNP: rs183886250
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 RCV002116514 SCV002446448 benign not provided 2024-01-31 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002500197 SCV002810266 likely benign Fraser syndrome 1 2021-09-14 criteria provided, single submitter clinical testing

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