ClinVar Miner

Submissions for variant NM_170675.5(MEIS2):c.964C>G (p.Gln322Glu)

dbSNP: rs2058712732
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Centre de Biologie Pathologie Génétique, Centre Hospitalier Universitaire de Lille RCV001252071 SCV001427819 likely pathogenic Cardiac malformation, cleft lip/palate, microcephaly, and digital anomalies 2019-01-01 no assertion criteria provided clinical testing

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