ClinVar Miner

Submissions for variant NM_001172509.2(SATB2):c.844A>G (p.Ile282Val)

dbSNP: rs1688735770
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001034066 SCV001197391 benign Chromosome 2q32-q33 deletion syndrome 2019-09-26 criteria provided, single submitter clinical testing

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