ClinVar Miner

Submissions for variant NM_000384.3(APOB):c.830G>T (p.Gly277Val)

dbSNP: rs1057516137
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
Robarts Research Institute, Western University RCV000408790 SCV000484827 uncertain significance Hypercholesterolemia, familial, 1 criteria provided, single submitter clinical testing

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