ClinVar Miner

Submissions for variant NM_003722.5(TP63):c.*2719_*2720del

dbSNP: rs574327104
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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 RCV000332134 SCV000442563 likely benign TP63-Related Spectrum Disorders 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000372634 SCV000442564 likely benign Cleft Lip +/- Cleft Palate, Autosomal Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000278081 SCV000442565 likely benign Ectrodactyly 2016-06-14 criteria provided, single submitter clinical testing

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