ClinVar Miner

Submissions for variant NM_025074.7(FRAS1):c.9450G>T (p.Val3150=)

gnomAD frequency: 0.00004  dbSNP: rs372168929
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000294394 SCV000339658 uncertain significance not provided 2016-03-08 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000294394 SCV004529582 likely benign not provided 2024-02-14 criteria provided, single submitter clinical testing

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