ClinVar Miner

Submissions for variant NM_016120.4(RLIM):c.777G>A (p.Thr259=)

gnomAD frequency: 0.00572  dbSNP: rs148132680
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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000597432 SCV000707587 benign not specified 2017-04-05 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV000884376 SCV001027751 benign not provided 2017-11-18 criteria provided, single submitter clinical testing
CeGaT Center for Human Genetics Tuebingen RCV000884376 SCV001247739 likely benign not provided 2020-01-01 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV000884376 SCV005210623 likely benign not provided criteria provided, single submitter not provided

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