ClinVar Miner

Submissions for variant NM_025074.7(FRAS1):c.4958C>T (p.Pro1653Leu)

gnomAD frequency: 0.00134  dbSNP: rs6813102
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000177922 SCV000229883 benign not specified 2014-12-12 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000878735 SCV001021690 likely benign not provided 2024-11-09 criteria provided, single submitter clinical testing

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