ClinVar Miner

Submissions for variant NM_007356.3(LAMB4):c.350G>C (p.Arg117Thr)

gnomAD frequency: 0.00583  dbSNP: rs149874137
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
Breakthrough Genomics, Breakthrough Genomics RCV001573222 SCV005271259 benign not provided criteria provided, single submitter not provided
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001573222 SCV001798759 likely benign not provided no assertion criteria provided clinical testing
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001579768 SCV001808452 benign not specified no assertion criteria provided clinical testing

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