Variants from VIB Department of Molecular Genetics, University of Antwerp

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)

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	not provided	total
0	0	0	0	0	334	334

Gene and significance breakdown #

Total genes and gene combinations: 8

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Gene or gene combination	not provided	total
PSEN1	141	141
GRN	80	80
MAPT	61	61
APP	23	23
PSEN2	13	13
CHMP2B	10	10
GRN, LOC125177489	5	5
FAM171A2, GRN	1	1

Condition and significance breakdown #

Total conditions: 1

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Condition	not provided	total
not provided	334	334

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