ClinVar Miner

Submissions for variant NM_000478.6(ALPL):c.1451T>G (p.Met484Arg)

dbSNP: rs1558558939
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
Institute of Human Genetics, University of Wuerzburg RCV000678461 SCV000804524 likely pathogenic Low alkaline phosphatase no assertion criteria provided clinical testing

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