ClinVar Miner

Submissions for variant NM_170675.5(MEIS2):c.825dup (p.Arg276fs)

dbSNP: rs1555456994
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Molecular Genetics Laboratory, BC Children's and BC Women's Hospitals RCV000677393 SCV000803688 pathogenic Cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies 2017-10-13 no assertion criteria provided clinical testing

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