ClinVar Miner

Submissions for variant NM_001447.3(FAT2):c.7376G>A (p.Gly2459Glu)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Dr. med. U. Finckh, Human Genetics, Eurofins MVZ RCV003234870 SCV003932842 likely benign Spinocerebellar ataxia 45 criteria provided, single submitter clinical testing

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