ClinVar Miner

Submissions for variant NM_003659.4(AGPS):c.225C>G (p.Pro75=)

dbSNP: rs1685064821
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 RCV002179605 SCV002335576 likely benign not provided 2021-06-24 criteria provided, single submitter clinical testing

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