ClinVar Miner

Submissions for variant NM_174889.5(NDUFAF2):c.103del (p.Ile35fs)

dbSNP: rs1554076324
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000001662 SCV000021818 pathogenic Mitochondrial complex 1 deficiency, nuclear type 10 2010-10-01 no assertion criteria provided literature only

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