ClinVar Miner

Submissions for variant NM_017780.4(CHD7):c.831G>T (p.Pro277=)

dbSNP: rs775415630
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001450187 SCV001653787 likely benign CHARGE syndrome 2024-11-17 criteria provided, single submitter clinical testing

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