ClinVar Miner

Submissions for variant NM_013275.6(ANKRD11):c.7806+11C>T

dbSNP: rs777198327
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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 RCV002215271 SCV002362096 benign KBG syndrome 2025-01-03 criteria provided, single submitter clinical testing

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