ClinVar Miner

Submissions for variant NM_133259.4(LRPPRC):c.1092A>G (p.Ser364=)

gnomAD frequency: 0.00011  dbSNP: rs549364492
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
Invitae RCV001408362 SCV001610360 likely benign not provided 2024-01-11 criteria provided, single submitter clinical testing

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