ClinVar Miner

Submissions for variant NM_000159.4(GCDH):c.-35+17A>G

gnomAD frequency: 0.96351  dbSNP: rs7251834
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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 RCV001527144 SCV001738071 benign Glutaric aciduria, type 1 2021-06-10 criteria provided, single submitter clinical testing
GeneDx RCV001673109 SCV001889968 benign not provided 2015-03-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001673109 SCV005314744 benign not provided criteria provided, single submitter not provided

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