ClinVar Miner

Submissions for variant NM_001295.3(CCR1):c.903C>T (p.Tyr301=)

gnomAD frequency: 0.00162  dbSNP: rs141128686
Minimum review status: Collection method:
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 RCV000951250 SCV001097630 benign not provided 2018-08-21 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000951250 SCV005050275 likely benign not provided 2024-05-01 criteria provided, single submitter clinical testing CCR1: BP4, BP7
Breakthrough Genomics, Breakthrough Genomics RCV000951250 SCV005241738 benign not provided criteria provided, single submitter not provided

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