ClinVar Miner

Variants studied for Alzheimer disease, type 3

Coded as:
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than one submission, it may be counted in more than one significance column. If this is the case, the total number of variants will be less than the sum of the other cells.

pathogenic likely pathogenic uncertain significance likely benign benign total
34 3 1 0 0 38

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination pathogenic likely pathogenic uncertain significance total
PSEN1 34 3 1 38

Submitter and significance breakdown #

Total submitters: 7
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Submitter pathogenic likely pathogenic uncertain significance total
OMIM 27 0 0 27
GeneReviews 12 0 0 12
UCLA Clinical Genomics Center, UCLA 1 0 0 1
Foundation for Research in Genetics and Endocrinology,Institute of Human Genetics 0 0 1 1
Undiagnosed Diseases Network,NIH 0 1 0 1
Laboratorio de Biología Molecular,FLENI 0 1 0 1
Department of Psychiatry and Medical Psychology,Medical University Pleven 0 1 0 1

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