ClinVar Miner

Submissions for variant NM_003659.4(AGPS):c.1749T>C (p.Phe583=)

dbSNP: rs2105733153
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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 RCV001479793 SCV001684099 likely benign not provided 2019-12-30 criteria provided, single submitter clinical testing

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