ClinVar Miner

Submissions for variant NM_003392.7(WNT5A):c.684+18C>A

gnomAD frequency: 0.00003  dbSNP: rs1264331427
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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 RCV002121802 SCV002442879 likely benign not provided 2023-08-07 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002500233 SCV002813140 likely benign Autosomal dominant Robinow syndrome 1 2022-05-04 criteria provided, single submitter clinical testing

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