ClinVar Miner

Submissions for variant NM_005529.7(HSPG2):c.6228G>A (p.Gly2076=)

gnomAD frequency: 0.00002  dbSNP: rs769398456
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
Labcorp Genetics (formerly Invitae), Labcorp RCV000914762 SCV001059947 likely benign not provided 2023-12-28 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV000914762 SCV003809239 uncertain significance not provided 2019-03-17 criteria provided, single submitter clinical testing

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