ClinVar Miner

Submissions for variant NM_000169.3(GLA):c.137A>G (p.His46Arg)

dbSNP: rs398123203
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
Eurofins Ntd Llc (ga) RCV000173078 SCV000224162 pathogenic not provided 2018-07-11 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000173078 SCV003828243 likely pathogenic not provided 2022-04-04 criteria provided, single submitter clinical testing

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