ClinVar Miner

Submissions for variant NM_153818.1(PEX10):c.772G>C (p.Gly258Arg) (rs61736380)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000178398 SCV000230471 uncertain significance not provided 2018-09-18 criteria provided, single submitter clinical testing
Fulgent Genetics,Fulgent Genetics RCV000763844 SCV000894768 uncertain significance Peroxisome biogenesis disorder 6A; Peroxisome biogenesis disorder 6B 2018-10-31 criteria provided, single submitter clinical testing

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