ClinVar Miner

Submissions for variant NM_001440.4(EXTL3):c.2148+13C>T

gnomAD frequency: 0.00342  dbSNP: rs114775959
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV001512795 SCV001720258 benign not provided 2025-01-25 criteria provided, single submitter clinical testing

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