ClinVar Miner

Submissions for variant NM_001375883.1(GPR161):c.-45+481A>T

gnomAD frequency: 0.06974  dbSNP: rs73030230
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 RCV001730383 SCV005286444 benign not provided criteria provided, single submitter not provided
Clinical Genetics, Academic Medical Center RCV001730384 SCV001979041 benign not specified no assertion criteria provided clinical testing
Laboratory of Diagnostic Genome Analysis, Leiden University Medical Center (LUMC) RCV001730383 SCV001979784 likely benign not provided no assertion criteria provided clinical testing

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