ClinVar Miner

Submissions for variant NM_015693.4(INTU):c.2074T>G (p.Cys692Gly)

gnomAD frequency: 0.00835  dbSNP: rs34311863
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 RCV002160258 SCV002412439 benign not provided 2025-01-28 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002160258 SCV005303354 benign not provided criteria provided, single submitter not provided

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