ClinVar Miner

Submissions for variant NM_005529.7(HSPG2):c.765G>A (p.Pro255=)

gnomAD frequency: 0.00004  dbSNP: rs1334406616
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
Athena Diagnostics RCV001288203 SCV001475160 likely benign not provided 2020-05-21 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001288203 SCV004557775 likely benign not provided 2024-07-30 criteria provided, single submitter clinical testing

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