ClinVar Miner

Submissions for variant NM_002844.4(PTPRK):c.485A>G (p.Asn162Ser)

gnomAD frequency: 0.00562  dbSNP: rs61757812
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 RCV000974415 SCV001122237 benign not provided 2018-03-28 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000974415 SCV004160272 likely benign not provided 2023-04-01 criteria provided, single submitter clinical testing PTPRK: PP2, BS2

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