ClinVar Miner

Submissions for variant NM_003659.4(AGPS):c.735G>A (p.Leu245=)

dbSNP: rs952911907
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 RCV001501067 SCV001705871 likely benign not provided 2024-09-18 criteria provided, single submitter clinical testing

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