ClinVar Miner

Submissions for variant NM_003394.4(WNT10B):c.676C>T (p.Arg226Ter)

gnomAD frequency: 0.00001  dbSNP: rs763991433
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare RCV000625580 SCV000746079 likely pathogenic Split hand-foot malformation 6 2017-09-18 no assertion criteria provided clinical testing
Molecular Pathology and Genetics, King Abdulaziz Medical City, Ministry of National Guard - Health Affairs RCV000625580 SCV000929977 likely pathogenic Split hand-foot malformation 6 2019-02-04 no assertion criteria provided clinical testing

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