ClinVar Miner

Submissions for variant NM_002618.4(PEX13):c.937T>G (p.Trp313Gly)

dbSNP: rs61752113
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000416325 SCV000494070 pathogenic Peroxisome biogenesis disorder 11B 2018-08-13 no assertion criteria provided literature only

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