ClinVar Miner

Submissions for variant NM_003172.4(SURF1):c.772C>T (p.Pro258Ser)

dbSNP: rs1053850536
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Laboratory of Metabolic Disorders, Peking University First Hospital RCV000754102 SCV000732897 pathogenic Leigh syndrome 2018-04-05 no assertion criteria provided research

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