ClinVar Miner

Submissions for variant NM_000883.4(IMPDH1):c.1779-3C>T

gnomAD frequency: 0.00004  dbSNP: rs761367230
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 RCV000909829 SCV001054654 likely benign not provided 2024-04-17 criteria provided, single submitter clinical testing

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