ClinVar Miner

Submissions for variant NM_003722.4(TP63):c.*2789A>G

gnomAD frequency: 0.16767  dbSNP: rs11708746
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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 RCV000315027 SCV000484054 benign Ectrodactyly 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000362750 SCV000484055 benign TP63-Related Spectrum Disorders 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000270897 SCV000484056 benign Cleft Lip +/- Cleft Palate, Autosomal Dominant 2016-06-14 criteria provided, single submitter clinical testing

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