ClinVar Miner

Submissions for variant NM_005068.3(SIM1):c.817G>A (p.Asp273Asn)

dbSNP: rs2114540224
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 Leipzig Medical Center RCV001706813 SCV001934325 uncertain significance Obesity 2020-09-03 criteria provided, single submitter clinical testing

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