ClinVar Miner

Submissions for variant NM_017547.4(FOXRED1):c.632G>C (p.Gly211Ala)

dbSNP: rs536400690
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genomic Research Center, Shahid Beheshti University of Medical Sciences RCV000625871 SCV000746446 uncertain significance Mitochondrial complex I deficiency 2020-05-03 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV001433617 SCV001636408 likely benign not provided 2024-01-30 criteria provided, single submitter clinical testing
Revvity Omics, Revvity RCV003139953 SCV003828330 uncertain significance Mitochondrial complex 1 deficiency, nuclear type 19 2019-03-27 criteria provided, single submitter clinical testing

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