ClinVar Miner

Submissions for variant NM_017780.4(CHD7):c.5895-67A>G

gnomAD frequency: 0.00009  dbSNP: rs528151295
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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 RCV001497036 SCV001701750 likely benign CHARGE syndrome 2020-08-07 criteria provided, single submitter clinical testing

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