ClinVar Miner

Submissions for variant NM_001004356.3(FGFRL1):c.1349A>G (p.His450Arg)

gnomAD frequency: 0.00018  dbSNP: rs182915641
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 RCV000906292 SCV001050920 likely benign not provided 2024-09-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000906292 SCV005263638 likely benign not provided criteria provided, single submitter not provided

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