ClinVar Miner

Submissions for variant NM_001109878.2(TBX22):c.-2-7C>G

dbSNP: rs185298778
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Mendelics RCV000990886 SCV001141939 benign Cleft palate with or without ankyloglossia, X-linked 2019-05-28 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004704396 SCV005210679 likely benign not provided criteria provided, single submitter not provided
PreventionGenetics, part of Exact Sciences RCV003928637 SCV004742760 benign TBX22-related disorder 2019-08-15 no assertion criteria provided clinical testing This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).

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