ClinVar Miner

Variants studied for Asperger syndrome, X-linked, susceptibility to, 2

Included ClinVar conditions (2):
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 risk factor total
0 0 1 0 2 1 4

Gene and significance breakdown #

Total genes and gene combinations: 1
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Gene or gene combination uncertain significance benign risk factor total
NLGN4X 1 2 1 4

Submitter and significance breakdown #

Total submitters: 3
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Submitter uncertain significance benign risk factor total
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories 0 2 0 2
OMIM 0 0 1 1
Geisinger Autism and Developmental Medicine Institute,Geisinger Health System 1 0 0 1

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