ClinVar Miner

Submissions for variant NM_000550.3(TYRP1):c.627T>A (p.Gly209=)

gnomAD frequency: 0.00058  dbSNP: rs1800374
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
PreventionGenetics, part of Exact Sciences RCV000246836 SCV000305271 likely benign not specified criteria provided, single submitter clinical testing
Invitae RCV000934663 SCV001080390 benign not provided 2024-01-15 criteria provided, single submitter clinical testing

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