ClinVar Miner

Submissions for variant NM_024996.7(GFM1):c.873A>G (p.Ser291=)

gnomAD frequency: 0.00001  dbSNP: rs1446412201
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001480744 SCV001685067 likely benign not provided 2020-03-09 criteria provided, single submitter clinical testing

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