ClinVar Miner

Submissions for variant NM_000478.6(ALPL):c.1574G>A (p.Ter525=)

dbSNP: rs1644760126
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV005094316 SCV005827890 likely benign not provided 2024-09-13 criteria provided, single submitter clinical testing
Natera, Inc. RCV001279680 SCV001466796 uncertain significance Hypophosphatasia 2020-08-13 no assertion criteria provided clinical testing

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