ClinVar Miner

Submissions for variant NM_000550.3(TYRP1):c.306C>T (p.Asn102=)

gnomAD frequency: 0.00205  dbSNP: rs145152954
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 RCV000897961 SCV001042139 benign not provided 2024-01-25 criteria provided, single submitter clinical testing
Genetic Services Laboratory, University of Chicago RCV001818731 SCV002071537 likely benign not specified 2021-06-14 criteria provided, single submitter clinical testing

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