ClinVar Miner

Submissions for variant NM_000191.3(HMGCL):c.-91G>T

dbSNP: rs6697805
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001533677 SCV001750437 benign Deficiency of hydroxymethylglutaryl-CoA lyase 2021-07-01 criteria provided, single submitter clinical testing
GeneDx RCV001685449 SCV001899241 benign not provided 2018-06-23 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001685449 SCV005282085 benign not provided criteria provided, single submitter not provided

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