ClinVar Miner

Submissions for variant NM_005297.4(MCHR1):c.530C>T (p.Pro177Leu)

gnomAD frequency: 0.00001  dbSNP: rs762669619
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
Genome Diagnostics Laboratory, Amsterdam University Medical Center RCV001579405 SCV001807116 uncertain significance not provided no assertion criteria provided clinical testing
Clinical Genetics, Academic Medical Center RCV001579405 SCV001917932 uncertain significance not provided no assertion criteria provided clinical testing

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