ClinVar Miner

Submissions for variant NC_000005.10:g.132369028T>G

gnomAD frequency: 0.06993  dbSNP: rs34786243
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 RCV001518453 SCV001727148 benign Renal carnitine transport defect 2025-01-13 criteria provided, single submitter clinical testing

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