ClinVar Miner

Submissions for variant NM_181882.3(PRX):c.164G>A (p.Arg55Lys)

dbSNP: rs773586301
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
CeGaT Center for Human Genetics Tuebingen RCV001531898 SCV001747221 uncertain significance not provided 2021-06-01 criteria provided, single submitter clinical testing

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