ClinVar Miner

Submissions for variant NM_012193.4(FZD4):c.729C>T (p.Ile243=)

gnomAD frequency: 0.00001  dbSNP: rs560649393
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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) RCV000175839 SCV000227405 uncertain significance not provided 2015-03-16 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000175839 SCV002463526 likely benign not provided 2022-11-15 criteria provided, single submitter clinical testing

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