ClinVar Miner

Submissions for variant NM_032861.4(SERAC1):c.487+19C>T

gnomAD frequency: 0.00009  dbSNP: rs372997779
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001519159 SCV001727980 benign 3-methylglutaconic aciduria with deafness, encephalopathy, and Leigh-like syndrome 2022-05-25 criteria provided, single submitter clinical testing

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