ClinVar Miner

Submissions for variant NM_004608.4(TBX6):c.353+9C>A

gnomAD frequency: 0.00165  dbSNP: rs369603655
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000733928 SCV000862033 uncertain significance not provided 2018-06-29 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000733928 SCV001042151 benign not provided 2023-10-23 criteria provided, single submitter clinical testing

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