ClinVar Miner

Submissions for variant NM_001366722.1(GRIP1):c.2886G>A (p.Pro962=)

gnomAD frequency: 0.00038  dbSNP: rs375330927
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Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV000897863 SCV001042033 likely benign not provided 2024-01-28 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002502633 SCV002806587 likely benign Fraser syndrome 3 2021-08-20 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000897863 SCV005216093 likely benign not provided criteria provided, single submitter not provided

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