ClinVar Miner

Submissions for variant NM_001126121.2(SLC25A19):c.373G>A (p.Gly125Ser)

dbSNP: rs387906944
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000023554 SCV000044845 pathogenic Progressive demyelinating neuropathy with bilateral striatal necrosis 2009-09-01 no assertion criteria provided literature only
GeneReviews RCV001847622 SCV002106342 not provided Amish lethal microcephaly no assertion provided literature only

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