ClinVar Miner

Submissions for variant NM_003221.4(TFAP2B):c.*912CA[6]

dbSNP: rs35649205
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000280865 SCV000463919 benign Char syndrome 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000280865 SCV000463922 uncertain significance Char syndrome 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001636986 SCV001849547 benign not provided 2021-05-16 criteria provided, single submitter clinical testing

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