ClinVar Miner

Submissions for variant NM_000021.4(PSEN1):c.495G>C (p.Trp165Cys)

dbSNP: rs63751484
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
VIB Department of Molecular Genetics, University of Antwerp RCV000084320 SCV000116456 not provided not provided no assertion provided not provided

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