ClinVar Miner

Submissions for variant NM_004168.4(SDHA):c.1908+90A>G

gnomAD frequency: 0.25155  dbSNP: rs6888536
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
Mendelics RCV000987497 SCV001136801 benign Mitochondrial complex II deficiency, nuclear type 1 2019-05-28 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004716651 SCV005302893 benign not provided criteria provided, single submitter not provided

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