ClinVar Miner

Variants studied for Early-Onset Familial Alzheimer Disease

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
0 0 106 47 0 153

Gene and significance breakdown #

Total genes and gene combinations: 3
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Gene or gene combination uncertain significance likely benign total
PSEN1 56 19 75
APP 29 13 42
PSEN2 21 15 36

Submitter and significance breakdown #

Total submitters: 1
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Submitter uncertain significance likely benign total
Illumina Clinical Services Laboratory,Illumina 106 47 153

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