ClinVar Miner

Submissions for variant NM_003392.7(WNT5A):c.522G>T (p.Pro174=)

gnomAD frequency: 0.00019  dbSNP: rs559836923
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002214796 SCV002361412 likely benign not provided 2023-11-02 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002498238 SCV002807547 likely benign Autosomal dominant Robinow syndrome 1 2021-09-20 criteria provided, single submitter clinical testing

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