ClinVar Miner

Submissions for variant NM_012193.4(FZD4):c.1194T>C (p.Tyr398=)

gnomAD frequency: 0.00093  dbSNP: rs147766472
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
Eurofins Ntd Llc (ga) RCV000267620 SCV000336297 uncertain significance not provided 2015-10-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000267620 SCV001046351 benign not provided 2024-01-20 criteria provided, single submitter clinical testing

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